Substituted dihydropyrrolopyrazole compound

ABSTRACT

Methods of producing a compound represented by formula (I) or a pharmacologically acceptable salt thereof include: 
                         
wherein L 1  is an optionally substituted C 1-6  alkylene group or the like, L 2  is a single bond or the like, L 3  is a single bond or the like, R 1 , R 2 , and R 3  are each independently an optionally substituted C 1-4  alkyl group or the like, R 4  is a hydrogen atom or the like, and R 5  is a hydrogen atom or the like.

This application is a divisional of application Ser. No. 15/522,592 filed Apr. 27, 2017, which is a National Stage Application of PCT/JP2015/080727 filed Oct. 30, 2015 and claims the benefit of Japanese Application No. 2014-223221 filed Oct. 31, 2014. The entire disclosures of the prior applications are hereby incorporated by reference herein their entirety.

TECHNICAL FIELD

The present invention relates to a substituted dihydropyrrolopyrazole compound or a pharmacologically acceptable salt thereof which has excellent CDK7 inhibitory activity and is useful as a medicament (e.g., a medicament for the treatment or prevention of cancers or inflammatory diseases), or a prodrug thereof.

BACKGROUND ART

CDKs (cyclin-dependent kinases) are cell growth control factors that are involved in entry to DNA synthesis (S phase) of the cell cycle and a mitotic phase (M phase), etc., and many types of CDKs are known. Also, the activation of CDK is controlled in multiple stages through the phosphorylation or dephosphorylation of the threonine residue of active loop (T loop) in its three-dimensional structure. When the particular threonine residue of CDK is phosphorylated, it forms a complex with a particular cyclin and is activated. This complex, which is important for cell cycle control, includes CDK1, CDK2/cyclin A, CDK1/cyclins B1 to B3 and CDK2, CDK4, CDK5, CDK6/cyclin D1 to D3, and CDK2/cyclin E, which are respectively involved in the particular periods of the cell cycle. CDK7 forms a CDK-activating kinase (CAK) together with cyclin H and MAT1 in metazoans and participates in the phosphorylation of CDKs (e.g., CDK1, CDK2, CDK4, and CDK6) necessary for the progression of the cell cycle (see Non Patent Literature 1).

Cell overgrowth by the abnormal activation of CDKs is a common feature in many cancers, and it is known that this is associated with a loss of checkpoint functions involved in the cell cycle control of cancer cells (see Non Patent Literature 2). Also, CDKs are known to have functions other than cell cycle control, and CDK7 is known to promote the binding of RNA polymerase II (RNAPII) to DNA and elongation thereof to positively control the transcription through the phosphorylation of serine in the COOH-terminal domain of the RNAPII (see Non Patent Literature 3).

CDK7 inhibitors exhibit effects in cell growth tests of various cancer cells and cancer-bearing mouse models, and the inhibition is expected to be useful as anticancer agents (see Non Patent Literatures 4 and 5).

Furthermore, it has been reported that in collagen-induced rheumatism mouse models, amelioration of clinical scores or tissue damage, decrease in the levels of inflammation-induced cytokines such as IL-6, IL-1β, and IL-17, and anti-CII-IgG2α, and decrease in the proportion of Th17 cells are attained by inhibiting CDK7 (see Non Patent Literature 6).

The CDK7 inhibitors, which play an important role in the progression of the cell cycle, are further expected to also have effects on the suppression of infection by viruses such as HIV, EBV, and HCV, and cardiomegaly (see Non Patent Literatures 7 and 8). Examples of diseases for which the CDK7 inhibitors seem to be useful, in addition to those described above, include autoimmune diseases typified by psoriasis and multiple sclerosis, neurodegenerative diseases typified by Alzheimer's disease, etc., allergic diseases typified by atopic dermatitis, etc., chronic respiratory diseases typified by chronic obstructive pulmonary disease (COPD), etc., and fibrosis typified by idiopathic pulmonary fibrosis, etc. (see Non Patent Literatures 9 to 11 and Non Patent Literatures 16 to 18).

Although the development of many CDK inhibitors is currently underway, there are not many compounds having an excellent CDK7 inhibitory effect (see Non Patent Literature 15).

CITATION LIST Patent Literature

-   Patent Literature 1: WO 2002/012242 -   Patent Literature 2: WO 2004/056827 -   Patent Literature 3: WO 2004/080457 -   Patent Literature 4: WO 2007/068637 -   Patent Literature 5: WO 2007/072153 -   Patent Literature 6: WO 2007/099171 -   Patent Literature 7: WO 2008/043745 -   Patent Literature 8: WO 2008/125945 -   Patent Literature 9: WO 2011/044264 -   Patent Literature 10: WO 2008/151304 -   Patent Literature 11: WO 2013/128028 -   Patent Literature 12: WO 2013/128029 -   Patent Literature 13: WO 2014/063068 -   Patent Literature 14: WO 2015/058126 -   Patent Literature 15: WO 2015/058140 -   Patent Literature 16: WO 2015/058163 -   Patent Literature 17: WO 2015/124941 -   Patent Literature 18: WO 2015/154022 -   Patent Literature 19: WO 2015/154038 -   Patent Literature 20: WO 2015/154039

Non Patent Literature

-   Non Patent Literature 1: Journal of Cell Science 2005, 118 (20),     5171-5180 -   Non Patent Literature 2: Nature Reviews Cancer 2009, 9, 153-166 -   Non Patent Literature 3: Biochim Biophys Acta 2004, 1677, 64-73 -   Non Patent Literature 4: Nature 2014, 511, 616-620 -   Non Patent Literature 5: Cancer Res 2009, 69, 6208-6215 -   Non Patent Literature 6: Clinical and Experimental Medicine, 2015,     15, 269-275 -   Non Patent Literature 7: Curr HIV Res 2003, 1 (2), 131-152 -   Non Patent Literature 8: Mol Cell Biol 1998, 18 (11), 6729-6736 -   Non Patent Literature 9: Br J Dermatol 2000, 143 (5), 950-956 -   Non Patent Literature 10: Biochem Biophys Res Commun 2013, 435 (3),     378-384 -   Non Patent Literature 11: Neurobiol Aging 2000, 6, 807-813 -   Non Patent Literature 12: Journal of Medicinal Chemistry 2012, 55     (10), 4728-4739 -   Non Patent Literature 13: Bioorganic & Medicinal Chemistry 2010, 18     (5), 1844-1853 -   Non Patent Literature 14: ChemMedChem 2007, 2, 841-852 -   Non Patent Literature 15: Current Drug Targets, 2010, 11, 291-302 -   Non Patent Literature 16: Clinical & Experimental Allergy, 2011, 41,     673-687 -   Non Patent Literature 17: Cell Death and Differentiation, 2012, 19,     1950-1961 -   Non Patent Literature 18: Am. J. Physiol. Lung Cell Mol, 2004, 286,     727-733

SUMMARY OF INVENTION Technical Problem

The present inventors have conducted studies on novel substituted dihydropyrrolopyrazole compounds with the aim of developing excellent CDK7 inhibitors and completed the present invention by finding that a novel substituted dihydropyrrolopyrazole compound having a particular structure or a pharmacologically acceptable salt thereof has excellent CDK7 inhibitory activity and is useful as a medicament (e.g., a medicament for the treatment or prevention of cancers or inflammatory diseases), and further finding even a compound that can serve as a prodrug of the compound.

Patent Literatures 1 to 9 and Non Patent Literatures 12 to 14 describe a compound having a 6,6-dimethyl-4,6-dihydropyrrolo[3,4-c]pyrazole skeleton, but do not disclose the compound according to the present invention or the pharmacologically acceptable salt thereof.

As compounds inhibiting CDK7, pyrazolopyrimidine derivatives are disclosed in Patent Literature 10, pyrazolotriazine derivatives are disclosed in Patent Literatures 11 and 12, phenyl derivatives are disclosed in Patent Literature 13 and Non Patent Literature 4, and heterocyclic compounds are disclosed in Patent Literatures 14 to 20; however, a compound having a 4,6-dihydropyrrolo[3,4-c]pyrazole skeleton is not disclosed.

Solution to Problem

The present invention provides a novel substituted dihydropyrrolopyrazole compound or a pharmacologically acceptable salt thereof which has excellent CDK7 inhibitory activity, or a prodrug thereof;

a pharmaceutical composition, preferably a pharmaceutical composition for the treatment or prevention of cancers, inflammatory diseases (e.g., autoimmune diseases), infection by viruses (HIV, EBV, HCV, etc.), neurodegenerative diseases (e.g., Alzheimer's disease), allergic diseases (e.g., atopic dermatitis), chronic respiratory diseases (e.g., chronic obstructive pulmonary disease (COPD)), fibrosis (e.g., idiopathic pulmonary fibrosis), circulatory diseases such as cardiomegaly, or impotence, comprising the substituted dihydropyrrolopyrazole compound or the pharmacologically acceptable salt thereof, or the prodrug thereof as an active ingredient; use of the substituted dihydropyrrolopyrazole compound or the pharmacologically acceptable salt thereof, or the prodrug thereof for the production of a pharmaceutical composition for the treatment or prevention (preferably, treatment) of diseases (preferably, the diseases described above); a method for treating or preventing (preferably, treating) diseases (preferably, the diseases described above) by administering a pharmaceutically effective amount of the substituted dihydropyrrolopyrazole compound or the pharmacologically acceptable salt thereof, or the prodrug thereof to a warm-blooded animal (preferably, a human); and a method for producing the substituted dihydropyrrolopyrazole compound or the pharmacologically acceptable salt thereof, or the prodrug thereof, or an intermediate thereof.

Examples of the cancers include urinary bladder cancer, breast cancer, large intestine cancer (e.g., colorectal cancer, for example, colon adenocarcinoma and colon adenoma), gastrointestinal stromal tumor, kidney cancer, epidermal cancer, liver cancer, lung cancer (e.g., adenocarcinoma, small-cell lung cancer, and non-small cell lung cancer), esophageal cancer, gallbladder cancer, ovary cancer, pancreatic cancer (e.g., exocrine pancreatic tumor), gastric cancer, cervical cancer, endometrial cancer, thyroid gland cancer, cancer of the nose, head and neck cancer, prostate cancer, skin cancer (e.g., squamous cell cancer), hematopoietic organ tumors of the lymphatic system (e.g., leukemia, acute lymphatic leukemia, chronic lymphatic leukemia, B cell lymphoma (e.g., diffuse large B cell lymphoma), T cell lymphoma, multiple myeloma, Hodgkin's lymphoma, non-Hodgkin's lymphoma, hairy cell lymphoma, and Burkitt's lymphoma), hematopoietic organ tumors of the myeloid system (e.g., acute or chronic myeloid leukemia, myelodysplastic syndrome, and promyelocytic leukemia), follicular carcinoma of thyroid, mesenchymal tumors (e.g., fibrosarcoma, Ewing's sarcoma, and rhabdomyosarcoma), tumors of the central or peripheral nervous system (e.g., astrocytoma, neuroblastoma, glioma, brain tumor, and schwannoma), melanoma, seminoma, teratoma, osteosarcoma, xeroderma pigmentosum, keratoacanthoma, follicular carcinoma of thyroid, and Kaposi's sarcoma.

Examples of the autoimmune diseases include multiple sclerosis, Guillain-Barre syndrome, myasthenia gravis, chronic atrophic gastritis, autoimmune hepatitis, primary biliary cirrhosis, ulcerative colitis, Crohn's disease, primary sclerosing cholangitis, autoimmune pancreatitis, aortitis syndrome, Goodpasture's syndrome, rapidly progressive glomerulonephritis, megaloblastic anemia, autoimmune hemolytic anemia, autoimmune neutropenia, idiopathic thrombocytopenic purpura, Graves' disease, Hashimoto disease, primary hypothyroidism, idiopathic Addison's disease, type 1 diabetes mellitus, circumscribed scleroderma, epidermolysis bullosa acquisita, vitiligo vulgaris, autoimmune optic neuropathy, autoimmune inner ear disorder, idiopathic azoospermia, rheumatoid arthritis, systemic lupus erythematosus, drug-induced lupus erythematosus, Sjogren's syndrome, polymyositis, psoriasis, dermatomyositis, scleroderma, vasculitis syndrome, mixed connective-tissue disease, and inflammatory bowel disease. In this context, the inflammatory bowel disease (IBD) is a generic name for diseases that cause chronic inflammation or ulcer in the large intestinal or small intestinal mucosa, and examples thereof include Crohn disease and ulcerative colitis.

In one aspect, the present invention provides the following [1] to [24]:

[1] A compound represented by formula (I) or a pharmacologically acceptable salt thereof:

wherein

L¹ is an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

L² is a single bond, an oxygen atom, an optionally substituted nitrogen atom, an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

L³ is a single bond, an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

R¹, R², and R³ are each independently an optionally substituted linear or branched C₁₋₄ alkyl group, an optionally substituted linear or branched C₂₋₄ alkenyl group, an optionally substituted linear or branched C₂₋₄ alkynyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group,

R⁴ is a hydrogen atom, an optionally substituted linear or branched C₁₋₆ alkyl group, an optionally substituted linear or branched C₂₋₆ alkenyl group, an optionally substituted linear or branched C₂₋₆ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₃₋₆ cycloalkenyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group, and

R⁵ is a hydrogen atom, an optionally substituted linear or branched C₁₋₁₆ alkyl group, an optionally substituted linear or branched C₂₋₁₆ alkenyl group, an optionally substituted linear or branched C₂₋₁₆ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₃₋₆ cycloalkenyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group.

[2] The compound or a pharmacologically acceptable salt thereof according to [1], wherein L¹ is an optionally substituted linear or branched C₁₋₆ alkylene group or an optionally substituted C₃₋₆ cycloalkylene group.

[3] A compound represented by formula (II) or a pharmacologically acceptable salt thereof:

wherein

L² is a single bond, an oxygen atom, an optionally substituted nitrogen atom, an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

L³ is a single bond, an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

R¹, R², and R³ are each independently an optionally substituted linear or branched C₁₋₄ alkyl group, an optionally substituted linear or branched C₂₋₄ alkenyl group, an optionally substituted linear or branched C₂₋₄ alkynyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group,

R⁴ is a hydrogen atom, an optionally substituted linear or branched C₁₋₆ alkyl group, an optionally substituted linear or branched C₂₋₆ alkenyl group, an optionally substituted linear or branched C₂₋₆ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₃₋₆ cycloalkenyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group, and

R⁵ is a hydrogen atom, an optionally substituted linear or branched C₁₋₁₆ alkyl group, an optionally substituted linear or branched C₂₋₁₆ alkenyl group, an optionally substituted linear or branched C₂₋₁₆ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₃₋₆ cycloalkenyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group.

[4] The compound or a pharmacologically acceptable salt thereof according to [3], wherein R¹, R², and R³ are each independently an optionally substituted linear or branched C₁₋₄ alkyl group.

[5] A compound represented by formula (III) or a pharmacologically acceptable salt thereof:

wherein

L² is a single bond, an oxygen atom, an optionally substituted nitrogen atom, an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

L³ is a single bond, an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

R¹, R², and R³ are each independently an optionally substituted linear or branched C₁₋₄ alkyl group, an optionally substituted linear or branched C₂₋₄ alkenyl group, an optionally substituted linear or branched C₂₋₄ alkynyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group,

R⁴ is a hydrogen atom, an optionally substituted linear or branched C₁₋₆ alkyl group, an optionally substituted linear or branched C₂₋₆ alkenyl group, an optionally substituted linear or branched C₂₋₆ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₃₋₆ cycloalkenyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group, and

R⁵ is a hydrogen atom, an optionally substituted linear or branched C₁₋₁₆ alkyl group, an optionally substituted linear or branched C₂₋₁₆ alkenyl group, an optionally substituted linear or branched C₂₋₁₆ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₃₋₆ cycloalkenyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group.

[6] The compound or a pharmacologically acceptable salt thereof according to [5], wherein R¹, R², and R³ are each independently an optionally substituted linear or branched C₁₋₄ alkyl group.

[7] A compound represented by formula (IV) or a pharmacologically acceptable salt thereof:

wherein

L² is a single bond, an oxygen atom, an optionally substituted nitrogen atom, an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

L³ is a single bond, an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

R¹, R², and R³ are each independently an optionally substituted linear or branched C₁₋₄ alkyl group, an optionally substituted linear or branched C₂₋₄ alkenyl group, an optionally substituted linear or branched C₂₋₄ alkynyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group,

R⁴ is a hydrogen atom, an optionally substituted linear or branched C₁₋₆ alkyl group, an optionally substituted linear or branched C₂₋₆ alkenyl group, an optionally substituted linear or branched C₂₋₆ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₃₋₆ cycloalkenyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group, and

R⁵ is a hydrogen atom, an optionally substituted linear or branched C₁₋₁₆ alkyl group, an optionally substituted linear or branched C₂₋₁₆ alkenyl group, an optionally substituted linear or branched C₂₋₁₆ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₃₋₆ cycloalkenyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group.

[8] The compound or a pharmacologically acceptable salt thereof according to [7], wherein R¹, R², and R³ are each independently an optionally substituted linear or branched C₁₋₄ alkyl group.

[9] A compound represented by formula (V) or (VI) or a pharmacologically acceptable salt thereof:

wherein

L¹ is an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

L² is a single bond, an oxygen atom, an optionally substituted nitrogen atom, an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

L³ is a single bond, an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

R¹, R², and R³ are each independently an optionally substituted linear or branched C₁₋₄ alkyl group, an optionally substituted linear or branched C₂₋₄ alkenyl group, an optionally substituted linear or branched C₂₋₄ alkynyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group,

R⁴ is a hydrogen atom, an optionally substituted linear or branched C₁₋₆ alkyl group, an optionally substituted linear or branched C₂₋₆ alkenyl group, an optionally substituted linear or branched C₂₋₆ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₃₋₆ cycloalkenyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group, and

R⁶ is a hydrogen atom, an optionally substituted linear or branched C₁₋₁₆ alkyl group, an optionally substituted linear or branched C₂₋₁₆ alkenyl group, an optionally substituted linear or branched C₂₋₁₆ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₃₋₆ cycloalkenyl group, an optionally substituted linear or branched C₁₋₆ alkoxy group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group,

R⁷ is an optionally substituted linear or branched C₁₋₁₆ alkyl group, an optionally substituted linear or branched C₂₋₁₆ alkenyl group, an optionally substituted linear or branched C₂₋₁₆ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₃₋₆ cycloalkenyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group, and

R⁸ and R⁹ are each independently a hydrogen atom or a C₁₋₄ alkyl group.

[10] The compound or a pharmacologically acceptable salt thereof according to [9], wherein L¹ is an optionally substituted linear or branched C₁₋₆ alkylene group or an optionally substituted C₃₋₆ cycloalkylene group, and R¹, R², and R³ are each independently an optionally substituted linear or branched C₁₋₄ alkyl group. [11] A compound selected from a compound group consisting of

-   (S)—N-(2-hydroxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-hydroxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-hydroxy-1-phenylethyl)-6,6-dimethyl-3-[2-methyl-2-(trimethylsilyl)propaneamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)-3-[1-(ethyldimethylsilyl)cyclobutanecarboxamido]-N-(2-hydroxy-1-phenylethyl)-6,6-dimethyl-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)-3-[2-(ethyldimethylsilyl)-2-methylpropaneamido]-N-(2-hydroxy-1-phenylethyl)-6,6-dimethyl-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-hydroxy-1-phenylethyl)-N,6,6-trimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)-2-[(2-m     ethoxypropan-2-yl)oxy]-1-phenylethyl6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate, -   (S)-2-hydroxy-1-phenylethyl -   6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate, -   2-Methoxy-1-phenylethyl -   6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate, -   N-[5-(4-hydroxy-3-phenylbutanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[5-(3-hydroxy-3-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)—N-(3-hydroxy-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(3-hydroxy-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(4-hydroxy-1-phenylbutyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(5-hydroxy-1-phenylpentyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-hydroxy-2-methyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-hydroxy-2-methyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(3-hydroxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(3-hydroxy-3-methyl-1-phenylbutyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-methoxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-[2-(difluoromethoxy)-1-phenylethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-ethoxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(3-methoxy-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   Sodium -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylacetate, -   (R)—N-(2-hydroxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[1-(2-fluorophenyl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-[1-(3-fluorophenyl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-[1-(4-fluorophenyl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[2-hydroxy-1-(pyridin-2-yl)ethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[2-hydroxy-1-(pyridin-3-yl)ethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[1-(benzo[d][1,3]dioxol-4-yl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(1-cyclohexyl-2-hydroxyethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(1-hydroxy-3-methylbutan-2-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(1-hydroxypropan-2-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(2-hydroxyethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(2-hydroxy-2-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(2-hydroxypropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[(2S)-1-hydroxy-3-methyl-1-phenylbutan-2-yl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(4-hydroxy-1-phenyl-2-butyn-1-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     acetate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     propionate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     butanoate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     pentanoate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     octanoate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     dodecanoate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     palmitate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     isobutanoate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     pivalate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     3-methyl butanoate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     benzoate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     ethyl carbonate, -   Sodium -   (S)-4-(2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethoxy)-4-oxobutanoate, -   (S)-(2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethoxy)methyl     pivalate, -   (S)-2-acetoxy-1-phenylethyl -   6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate, -   (S)-benzyl -   2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylacetate, -   (S)-methyl -   2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylacetate, -   N-(2,2-difluoro-3-hydroxy-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(2-isopropoxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   6,6-Dimethyl-N-(2-phenoxy-1-phenylethyl)-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-[1-(2-chlorophenyl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-[2-hydroxy-1-(o-tolyl)ethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(1-hydroxy-3-phenylpropan-2-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(2-hydroxy-3-methylbutyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(1-hydroxy-3-phenylpropan-2-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(2-hydroxy-2-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-hydroxy-2-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   2-Hydroxy-2-phenylethyl -   6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate, -   (R)—N-[6,6-dimethyl-5-(2-phenoxypropanoyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (S)—N-[6,6-dimethyl-5-(2-phenoxypropanoyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[6,6-dimethyl-5-(2-phenoxyacetyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)—N-[6,6-dimethyl-5-(2-phenoxypropanoyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclopropanecarboxamide, -   N-{5-[3-(benzyloxy)-2-phenoxypropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[5-(3-hydroxy-2-phenoxypropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[2-(4-chlorophenoxy)propanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[2-(2-chlorophenoxy)propanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[2-(cyclohexyloxy)propanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[2-(3-chlorophenoxy)propanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[5-(2-methoxypropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[5-(3-methoxy-2-phenoxypropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{6,6-dimethyl-5-[2-(pyridin-3-yloxy)propanoyl]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[3-(dimethylamino)-2-phenoxypropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[6,6-dimethyl-5-(2-phenoxy-2-phenylacetyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[3-(3,3-difluoropyrrolidin-1-yl)-2-phenoxypropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[5-(3-hydroxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (S)—N-[5-(3-hydroxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide -   (R)—N-{5-[3-(benzyloxy)-2-phenylpropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)—N-[5-(3-hydroxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide -   (R)—N-[5-(2-methoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (S)—N-[5-(2-methoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[5-(3-methoxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[5-(4-methoxy-2-phenylbutanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (S)—N-[5-(3-hydroxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclopropanecarboxamide, -   (R)—N-[5-(2-methoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclopropanecarboxamide, -   (R)—N-{5-[2-(difluoromethoxy)-2-phenylacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)—N-[5-(2-ethoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)-1-(ethyldimethylsilyl)-N-[5-(2-methoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]cyclobutanecarboxamide, -   (R)—N-[5-(2-cyclopropoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsiyl)cyclobutanecarboxamide, -   (R)—N-[5-(2-isopropoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsiyl)cyclobutanecarboxamide, -   (R)—N-{6,6-dimethyl-5-[2-phenyl-2-(trifluoromethoxy)acetyl]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)—N-[6,6-dimethyl-5-(2-phenyl-2-propoxyacetyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[2-(4-fluorophenyl)-2-methoxyacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[2-(3-fluorophenyl)-2-methoxyacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)—N-{5-[2-(2-fluorophenyl)-2-methoxyacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[2-methoxy-2-(thiophen-2-yl)acetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   (−)-N-{5-[2-methoxy-2-(thiophen-2-yl)acetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   (+)-N-{5-[2-methoxy-2-(thiophen-2-yl)acetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{[1-(hydroxymethyl)cyclobutyl](phenyl)methyl}-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-[2-(1-hydroxycyclopropyl)-1-phenylethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(3-ethyl-3-hydroxy-1-phenylpentyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-[1-(4-fluorophenyl)-3-hydroxy-3-methylbutyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-[1-(3-fluorophenyl)-3-hydroxy-3-methylbutyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-[1-(2-fluorophenyl)-3-hydroxy-3-methylbutyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(5-hydroxy-2,5-dimethylhexan-3-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[1-(4-fluorophenyl)-3-hydroxy2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[1-(3-fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (−)-N-[1-(3-fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (+)-N-[1-(3-fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[1-(2-fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(1-hydroxy-2,2,4-trimethylpentan-3-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(3-hydroxy-3-methyl-1-phenylbutyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(3-hydroxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (−)-N-(3-hydroxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (+)-N-(3-hydroxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-[5-(2-butoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide,     and -   N-(3-methoxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide -   or a pharmacologically acceptable salt thereof.     [12]     (R)—N-[1-(4-fluorophenyl)-3-hydroxy-3-methylbutyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide     or a pharmacologically acceptable salt thereof.     [13]     (−)-N-(3-hydroxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropane-1-carboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide     or a pharmacologically acceptable salt thereof.     [14]     (R)—N-[5-(2-methoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide     or a pharmacologically acceptable salt thereof.     [15]     (R)—N-[6,6-dimethyl-5-(2-phenyl-2-propoxyacetyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide     or a pharmacologically acceptable salt thereof.     [16]     (R)—N-{5-[2-(2-fluorophenyl)-2-methoxyacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide     or a pharmacologically acceptable salt thereof.     [17]     (R)—N-[5-(2-ethoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide     or a pharmacologically acceptable salt thereof.     [18]     (R)—N-[5-(2-cyclopropoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide     or a pharmacologically acceptable salt thereof.     [19]     (R)—N-[5-(2-isopropoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide     or a pharmacologically acceptable salt thereof.     [20]     (+)-N-{5-[2-methoxy-2-(thiophen-2-yl)acetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutane     carboxamide or a pharmacologically acceptable salt thereof.     [21]     (−)-N-[1-(3-fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide     or a pharmacologically acceptable salt thereof.     [22]     N-{5-[2-(3-fluorophenyl)-2-methoxyacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide     or a pharmacologically acceptable salt thereof.     [23]     N-[1-(4-fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide     or a pharmacologically acceptable salt thereof.     [24]     (R)—N-[1-(3-fluorophenyl)-3-hydroxy-3-methylbutyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide     or a pharmacologically acceptable salt thereof.     [25]     (R)—N-{6,6-dimethyl-5-[2-phenyl-2-(trifluoromethoxy)acetyl]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide     or a pharmacologically acceptable salt thereof.     [26]     (R)—N-[2-(1-hydroxycyclopropyl)-1-phenylethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide     or a pharmacologically acceptable salt thereof.     [27]     (R)—N-(3-hydroxy-3-methyl-1-phenylbutyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide     or a pharmacologically acceptable salt thereof.     [28]     (R)—N-[5-(2-methoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclopropanecarboxamide     or a pharmacologically acceptable salt thereof.     [29]     (R)—N-{5-[2-(difluoromethoxy)-2-phenylacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide     or a pharmacologically acceptable salt thereof.     [30]     (R)-1-(ethyldimethylsilyl)-N-[5-(2-methoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]cyclobutanecarboxamide     or a pharmacologically acceptable salt thereof.     [31]     N-{[1-(hydroxymethyl)cyclobutyl](phenyl)methyl}-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide     or a pharmacologically acceptable salt thereof.     [32] A pharmaceutical composition comprising the compound or a     pharmacologically acceptable salt thereof according to any of [1] to     [31].     [33] The pharmaceutical composition according to [32], wherein the     pharmaceutical composition is a CDK7 inhibitor or a prophylactic     agent.     [34] The pharmaceutical composition according to [32] or [33],     wherein the pharmaceutical composition is for treating or preventing     a cancer or an inflammatory disease.     [35] The pharmaceutical composition according to [34], wherein the     inflammatory disease is an autoimmune disease.     [36] The pharmaceutical composition according to [35], wherein the     autoimmune disease is rheumatoid arthritis or psoriasis.     [37] A method for treating or preventing a cancer or an inflammatory     disease, comprising administering the compound or the     pharmacologically acceptable salt thereof according to any of [1] to     [31] to a subject in need thereof.     [38] The method according to [37], wherein the inflammatory disease     is an autoimmune disease.     [39] The method according to [38], wherein the autoimmune disease is     rheumatoid arthritis or psoriasis.     [40] Use of the compound or the pharmacologically acceptable salt     thereof according to any of [1] to [31] for the production of a     pharmaceutical composition which is a CDK7 inhibitor or a     prophylactic agent.     [41] Use of the compound or the pharmacologically acceptable salt     thereof according to any of [1] to [31] for inhibiting CDK7.     [42] Use of the compound or the pharmacologically acceptable salt     thereof according to any of [1] to [31] for treating or preventing a     cancer or an inflammatory disease.     [43] Use according to [42], wherein the inflammatory disease is an     autoimmune disease.     [44] Use according to [43], wherein the autoimmune disease is     rheumatoid arthritis or psoriasis.     [45] The compound or the pharmacologically acceptable salt thereof     according to any of [1] to [31] for use as an active ingredient for     a pharmaceutical composition.     [46] The compound or the pharmacologically acceptable salt thereof     according to [45], wherein the pharmaceutical composition is a     pharmaceutical composition for the treatment of a cancer or an     inflammatory disease.     [47] The compound or the pharmacologically acceptable salt thereof     according to [46], wherein the inflammatory disease is an autoimmune     disease.     [48] The compound or the pharmacologically acceptable salt thereof     according to [47], wherein the autoimmune disease is rheumatoid     arthritis or psoriasis.

Specific examples of the compound represented by formula (I) of the present invention can include compounds as shown in Tables 1 to 164 described below. In Tables 1 to 164 described below, Me represents a methyl group, Et represents an ethyl group, nPr represents a n-propyl group, iPr represents an isopropyl group, cPr represents a cyclopropyl group, nBu represents a n-butyl group, iBu represents an isobutyl group, tBu represents a tert-butyl group, cHex represents a cyclohexyl group, Ph represents a phenyl group, 2-F-Ph represents a 2-fluorophenyl group, 3-F-Ph represents a 3-fluorophenyl group, 4-F-Ph represents a 4-fluorophenyl group, 2-Cl-Ph represents a 2-chlorophenyl group, 3-Cl-Ph represents a 3-chlorophenyl group, 4-Cl-Ph represents a 4-chlorophenyl group, 2-Me-Ph represents a 2-methylphenyl group, 3-Me-Ph represents a 3-methylphenyl group, 4-Me-Ph represents a 4-methylphenyl group, 2-Py represents a 2-pyridyl group, 3-Py represents a 3-pyridyl group, 4-Py represents a 4-pyridyl group, Bn represents a benzyl group, “—” represents a single bond, “(R)—” and “(S)—” each represent the configuration of a carbon atom with “*” in the following formulas (I), (II), (III), (IV), (Va), (Vb), (Vc), (VIa), (VIb), and (VIc), “racemic” represents being a racemate, “(+)” represents being a dextrorotatory optically active form, and “(−)” represents being a levorotatory optically active form. As for each chemical structure described as L¹, L², or L³ in the tables, the atom positioned on the left side of the chemical structure binds to a silicon atom, a carbonyl group, or a carbon atom with “*” in the corresponding formula. In the case of, for example, a compound of compound No. 1-21, CH₂—C(Me)₂ corresponding to L¹ means that the methylene carbon atom (CH₂) binds to a silicon atom and the quaternary carbon atom (C) binds to a carbonyl group, and C≡CCH₂ corresponding to L³ means that the quaternary carbon atom (C) binds to a carbon atom with “*” and the methylene carbon atom (CH₂) binds to an oxygen atom adjacent to R⁵.

TABLE 1 (I)

Com- pound Con- No. R¹ R² R³ L¹ L² R⁴ L³ R⁵ figuration I-1  Me Me Me CH₂ O Ph CH₂ H racemic I-2  Me Me Me CH₂ O Ph CH₂ H (S)- I-3  Me Me Me CH₂ O Ph CH₂ Me racemic I-4  Me Me Me CH₂ O Ph CH₂ Me (S)- I-5  Me Me Me CH₂ O Ph (CH₂)₂ H racemic I-6  Me Me Me CH₂ O Ph (CH₂)₂ H (R)- I-7  Me Me Me CH₂ O Ph (CH₂)₂ Me racemic I-8  Me Me Me CH₂ O Ph (CH₂)₂ Me (R)- I-9  Me Me Me CH₂ O Ph C≡CCH₂ H racemic I-10 Me Me Me CH₂ O Ph C≡CCH₂ H (S)- I-11 Me Me Me CH₂ O Ph C≡CCH₂ Me racemic I-12 Me Me Me CH₂ O Ph C≡CCH₂ Me (S)- I-13 Me Me Me CH₂C(Me)₂ O Ph CH₂ H racemic I-14 Me Me Me CH₂C(Me)₂ O Ph CH₂ H (S)- I-15 Me Me Me CH₂C(Me)₂ O Ph CH₂ Me racemic I-16 Me Me Me CH₂C(Me)₂ O Ph CH₂ Me (S)- I-17 Me Me Me CH₂C(Me)₂ O Ph (CH₂)₂ H racemic I-18 Me Me Me CH₂C(Me)₂ O Ph (CH₂)₂ H (R)- I-19 Me Me Me CH₂C(Me)₂ O Ph (CH₂)₂ Me racemic I-20 Me Me Me CH₂C(Me)₂ O Ph (CH₂)₂ Me (R)- I-21 Me Me Me CH₂C(Me)₂ O Ph C≡CCH₂ H racemic I-22 Me Me Me CH₂C(Me)₂ O Ph C≡CCH₂ H (S)- I-23 Me Me Me CH₂C(Me)₂ O Ph C≡CCH₂ Me racemic I-24 Me Me Me CH₂C(Me)₂ O Ph C≡CCH₂ Me (S)- I-25 Me Me Me CH₂CH═CH O Ph CH₂ H racemic I-26 Me Me Me CH₂CH═CH O Ph CH₂ H (S)- I-27 Me Me Me CH₂CH═CH O Ph CH₂ Me racemic I-28 Me Me Me CH₂CH═CH O Ph CH₂ Me (S)- I-29 Me Me Me CH₂CH═CH O Ph (CH₂)₂ H racemic I-30 Me Me Me CH₂CH═CH O Ph (CH₂)₂ H (R)- I-31 Me Me Me CH₂CH═CH O Ph (CH₂)₂ Me racemic I-32 Me Me Me CH₂CH═CH O Ph (CH₂)₂ Me (R)- I-33 Me Me Me CH₂CH═CH O Ph C≡CCH₂ H racemic I-34 Me Me Me CH₂CH═CH O Ph C≡CCH₂ H (S)- I-35 Me Me Me CH₂CH═CH O Ph C≡CCH₂ Me racemic I-36 Me Me Me CH₂CH═CH O Ph C≡CCH₂ Me (S)- I-37 Me Me Me CH₂C≡C O Ph CH₂ H racemic I-38 Me Me Me CH₂C≡C O Ph CH₂ H (S)- I-39 Me Me Me CH₂C≡C O Ph CH₂ Me racemic I-40 Me Me Me CH₂C≡C O Ph CH₂ Me (S)- I-41 Me Me Me CH₂C≡C O Ph (CH₂)₂ H racemic I-42 Me Me Me CH₂C≡C O Ph (CH₂)₂ H (R)- I-43 Me Me Me CH₂C≡C O Ph (CH₂)₂ Me racemic I-44 Me Me Me CH₂C≡C O Ph (CH₂)₂ Me (R)- I-45 Me Me Me CH₂C≡C O Ph C≡CCH₂ H racemic I-46 Me Me Me CH₂C≡C O Ph C≡CCH₂ H (S)- I-47 Me Me Me CH₂C≡C O Ph C≡CCH₂ Me racemic I-48 Me Me Me CH₂C≡C O Ph C≡CCH₂ Me (S)- I-49 Me Me Me 1,2-Cyclo- O Ph CH₂ H racemic propylene I-50 Me Me Me 1,2-Cyclo- O Ph CH₂ H (S)- propylene

TABLE 2 (I)

Com- Con- pound figu- No. R¹ R² R³ L¹ L² R⁴ L³ R⁵ ration I-51 Me Me Me 1,2-Cyclo- O Ph CH₂ Me racemic propylene I-52 Me Me Me 1,2-Cyclo- O Ph CH₂ Me (S)- propylene I-53 Me Me Me 1,2-Cyclo- O Ph (CH₂)₂ H racemic propylene I-54 Me Me Me 1,2-Cyclo- O Ph (CH₂)₂ H (R)- propylene I-55 Me Me Me 1,2-Cyclo- O Ph (CH₂)₂ Me racemic propylene I-56 Me Me Me 1,2-Cyclo- O Ph (CH₂)₂ Me (R)- propylene I-57 Me Me Me 1,2-Cyclo- O Ph C≡CCH₂ H racemic propylene I-58 Me Me Me 1,2-Cyclo- O Ph C≡CCH₂ H (S)- propylene I-59 Me Me Me 1,2-Cyclo- O Ph C≡CCH₂ Me racemic propylene I-60 Me Me Me 1,2-Cyclo- O Ph C≡CCH₂ Me (S)- propylene I-61 Me Me Me 5,5- O Ph CH₂ H racemic Spiro[2.3] hexylene I-62 Me Me Me 5,5- O Ph CH₂ H (S)- Spiro[2.3] hexylene I-63 Me Me Me 5,5- O Ph CH₂ Me racemic Spiro[2.3] hexylene I-64 Me Me Me 5,5- O Ph CH₂ Me (S)- Spiro[2.3] hexylene I-65 Me Me Me 5,5- O Ph (CH₂)₂ H racemic Spiro[2.3] hexylene I-66 Me Me Me 5,5- O Ph (CH₂)₂ H (R)- Spiro[2.3] hexylene I-67 Me Me Me 5,5- O Ph (CH₂)₂ Me racemic Spiro[2.3] hexylene I-68 Me Me Me 5,5- O Ph (CH₂)₂ Me (R)- Spiro[2.3] hexylene I-69 Me Me Me 5,5- O Ph C≡CCH₂ H racemic Spiro[2.3] hexylene I-70 Me Me Me 5,5- O Ph C≡CCH₂ H (S)- Spiro[2.3] hexylene I-71 Me Me Me 5,5- O Ph C≡CCH₂ Me racemic Spiro[2.3] hexylene I-72 Me Me Me 5,5- O Ph C≡CCH₂ Me (S)- Spiro[2.3] hexylene I-73 Me Me Me 4,4-Cyclo- O Ph CH₂ H racemic pentenylene I-74 Me Me Me 4,4-Cyclo- O Ph CH₂ H (S)- pentenylene I-75 Me Me Me 4,4-Cyclo- O Ph CH₂ Me racemic pentenylene I-76 Me Me Me 4,4-Cyclo- O Ph CH₂ Me (S)- pentenylene I-77 Me Me Me 4,4-Cyclo- O Ph (CH₂)₂ H racemic pentenylene I-78 Me Me Me 4,4-Cyclo- O Ph (CH₂)₂ H (R)- pentenylene I-79 Me Me Me 4,4-Cyclo- O Ph (CH₂)₂ Me racemic pentenylene I-80 Me Me Me 4,4-Cyclo- O Ph (CH₂)₂ Me (R)- pentenylene I-81 Me Me Me 4,4-Cyclo- O Ph C≡CCH₂ H racemic pentenylene I-82 Me Me Me 4,4-Cyclo- O Ph C≡CCH₂ H (S)- pentenylene I-83 Me Me Me 4,4-Cyclo- O Ph C≡CCH₂ Me racemic pentenylene I-84 Me Me Me 4,4-Cyclo- O Ph C≡CCH₂ Me (S)- pentenylene I-85 Me Me Me CH₂ NH Ph CH₂ H racemic I-86 Me Me Me CH₂ NH Ph CH₂ H (S)- I-87 Me Me Me CH₂ NH Ph CH₂ Me racemic I-88 Me Me Me CH₂ NH Ph CH₂ Me (S)- I-89 Me Me Me CH₂ NH Ph (CH₂)₂ H racemic I-90 Me Me Me CH₂ NH Ph (CH₂)₂ H (R)- I-91 Me Me Me CH₂ NH Ph (CH₂)₂ Me racemic I-92 Me Me Me CH₂ NH Ph (CH₂)₂ Me (R)- I-93 Me Me Me CH₂ NH Ph C≡CCH₂ H racemic I-94 Me Me Me CH₂ NH Ph C≡CCH₂ H (S)- I-95 Me Me Me CH₂ NH Ph C≡CCH₂ Me racemic I-96 Me Me Me CH₂ NH Ph C≡CCH₂ Me (S)- I-97 Me Me Me CH₂C(Me)₂ NH Ph CH₂ H racemic I-98 Me Me Me CH₂C(Me)₂ NH Ph CH₂ H (S)- I-99 Me Me Me CH₂C(Me)₂ NH Ph CH₂ Me racemic  I-100 Me Me Me CH₂C(Me)₂ NH Ph CH₂ Me (S)-

TABLE 3 (I)

Com- Con- pound figu- No. R¹ R² R³ L¹ L² R⁴ L³ R⁵ ration I-101 Me Me Me CH₂C(Me)₂ NH Ph (CH₂)₂ H racemic I-102 Me Me Me CH₂C(Me)₂ NH Ph (CH₂)₂ H (R)- I-103 Me Me Me CH₂C(Me)₂ NH Ph (CH₂)₂ Me racemic I-104 Me Me Me CH₂C(Me)₂ NH Ph (CH₂)₂ Me (R)- I-105 Me Me Me CH₂C(Me)₂ NH Ph C≡CCH₂ H racemic I-106 Me Me Me CH₂C(Me)₂ NH Ph C≡CCH₂ H (S)- I-107 Me Me Me CH₂C(Me)₂ NH Ph C≡CCH₂ Me racemic I-108 Me Me Me CH₂C(Me)₂ NH Ph C≡CCH₂ Me (S)- I-109 Me Me Me CH₂CH═CH NH Ph CH₂ H racemic I-110 Me Me Me CH₂CH═CH NH Ph CH₂ H (S)- I-111 Me Me Me CH₂CH═CH NH Ph CH₂ Me racemic I-112 Me Me Me CH₂CH═CH NH Ph CH₂ Me (S)- I-113 Me Me Me CH₂CH═CH NH Ph (CH₂)₂ H racemic I-114 Me Me Me CH₂CH═CH NH Ph (CH₂)₂ H (R)- I-115 Me Me Me CH₂CH═CH NH Ph (CH₂)₂ Me racemic I-116 Me Me Me CH₂CH═CH NH Ph (CH₂)₂ Me (R)- I-117 Me Me Me CH₂CH═CH NH Ph C≡CCH₂ H racemic I-118 Me Me Me CH₂CH═CH NH Ph C≡CCH₂ H (S)- I-119 Me Me Me CH₂CH═CH NH Ph C≡CCH₂ Me racemic I-120 Me Me Me CH₂CH═CH NH Ph C≡CCH₂ Me (S)- I-121 Me Me Me CH₂C≡C NH Ph CH₂ H racemic I-122 Me Me Me CH₂C≡C NH Ph CH₂ H (S)- I-123 Me Me Me CH₂C≡C NH Ph CH₂ Me racemic I-124 Me Me Me CH₂C≡C NH Ph CH₂ Me (S)- I-125 Me Me Me CH₂C≡C NH Ph (CH₂)₂ H racemic I-126 Me Me Me CH₂C≡C NH Ph (CH₂)₂ H (R)- I-127 Me Me Me CH₂C≡C NH Ph (CH₂)₂ Me racemic I-128 Me Me Me CH₂C≡C NH Ph (CH₂)₂ Me (R)- I-129 Me Me Me CH₂C≡C NH Ph C≡CCH₂ H racemic I-130 Me Me Me CH₂C≡C NH Ph C≡CCH₂ H (S)- I-131 Me Me Me CH₂C≡C NH Ph C≡CCH₂ Me racemic I-132 Me Me Me CH₂C≡C NH Ph C≡CCH₂ Me (S)- I-133 Me Me Me 1,2-Cyclo- NH Ph CH₂ H racemic propylene I-134 Me Me Me 1,2-Cyclo- NH Ph CH₂ H (S)- propylene I-135 Me Me Me 1,2-Cyclo- NH Ph CH₂ Me racemic propylene I-136 Me Me Me 1,2-Cyclo- NH Ph CH₂ Me (S)- propylene I-137 Me Me Me 1,2-Cyclo- NH Ph (CH₂)₂ H racemic propylene I-138 Me Me Me 1,2-Cyclo- NH Ph (CH₂)₂ H (R)- propylene I-139 Me Me Me 1,2-Cyclo- NH Ph (CH₂)₂ Me racemic propylene I-140 Me Me Me 1,2-Cyclo- NH Ph (CH₂)₂ Me (R)- propylene I-141 Me Me Me 1,2-Cyclo- NH Ph C≡CCH₂ H racemic propylene I-142 Me Me Me 1,2-Cyclo- NH Ph C≡CCH₂ H (S)- propylene I-143 Me Me Me 1,2-Cyclo- NH Ph C≡CCH₂ Me racemic propylene I-144 Me Me Me 1,2-Cyclo- NH Ph C≡CCH₂ Me (S)- propylene I-145 Me Me Me 5,5-Spiro[2.3] NH Ph CH₂ H racemic hexylene I-146 Me Me Me 5,5-Spiro[2.3] NH Ph CH₂ H (S)- hexylene I-147 Me Me Me 5,5-Spiro[2.3] NH Ph CH₂ Me racemic hexylene I-148 Me Me Me 5,5-Spiro[2.3] NH Ph CH₂ Me (S)- hexylene I-149 Me Me Me 5,5-Spiro[2.3] NH Ph (CH₂)₂ H racemic hexylene I-150 Me Me Me 5,5-Spiro[2.3] NH Ph (CH₂)₂ H (R)- hexylene

TABLE 4 (I)

Com- Con- pound figu- No. R¹ R² R³ L¹ L² R⁴ L³ R⁵ ration I-151 Me Me Me 5,5- NH Ph (CH₂)₂ Me racemic Spiro[2.3] hexylene I-152 Me Me Me 5,5- NH Ph (CH₂)₂ Me (R)- Spiro[2.3] hexylene I-153 Me Me Me 5,5- NH Ph C≡CCH₂ H racemic Spiro[2.3] hexylene I-154 Me Me Me 5,5- NH Ph C≡CCH₂ H (S)- Spiro[2.3] hexylene I-155 Me Me Me 5,5- NH Ph C≡CCH₂ Me racemic Spiro[2.3] hexylene I-156 Me Me Me 5,5- NH Ph C≡CCH₂ Me (S)- Spiro[2.3] hexylene I-157 Me Me Me 4,4-Cyclo- NH Ph CH₂ H racemic pentenylene I-158 Me Me Me 4,4-Cyclo- NH Ph CH₂ H (S)- pentenylene I-159 Me Me Me 4,4-Cyclo- NH Ph CH₂ Me racemic pentenylene I-160 Me Me Me 4,4-Cyclo- NH Ph CH₂ Me (S)- pentenylene I-161 Me Me Me 4,4-Cyclo- NH Ph (CH₂)₂ H racemic pentenylene I-162 Me Me Me 4,4-Cyclo- NH Ph (CH₂)₂ H (R)- pentenylene I-163 Me Me Me 4,4-Cyclo- NH Ph (CH₂)₂ Me racemic pentenylene I-164 Me Me Me 4,4-Cyclo- NH Ph (CH₂)₂ Me (R)- pentenylene I-165 Me Me Me 4,4-Cyclo- NH Ph C≡CCH₂ H racemic pentenylene I-166 Me Me Me 4,4-Cyclo- NH Ph C≡CCH₂ H (S)- pentenylene I-167 Me Me Me 4,4-Cyclo- NH Ph C≡CCH₂ Me racemic pentenylene I-168 Me Me Me 4,4-Cyclo- NH Ph C≡CCH₂ Me (S)- pentenylene I-169 Me Me Me CH₂ CH₂ Ph CH₂ H racemic I-170 Me Me Me CH₂ CH₂ Ph CH₂ H (S)- I-171 Me Me Me CH₂ CH₂ Ph — H racemic I-172 Me Me Me CH₂ CH₂ Ph — H (S)- I-173 Me Me Me CH₂ CH₂ Ph CH₂ Me racemic I-174 Me Me Me CH₂ CH₂ Ph CH₂ Me (S)- I-175 Me Me Me CH₂ CH₂ Ph C(Me)₂ H racemic I-176 Me Me Me CH₂ CH₂ Ph C(Me)₂ H (S)- I-177 Me Me Me CH₂ CH₂ Ph C(Me)₂ Me racemic I-178 Me Me Me CH₂ CH₂ Ph C(Me)₂ Me (S)- I-179 Me Me Me CH₂ CH₂ Ph (CH₂)₂ H racemic I-180 Me Me Me CH₂ CH₂ Ph (CH₂)₂ H (S)- I-181 Me Me Me CH₂ CH₂ Ph (CH₂)₂ Me racemic I-182 Me Me Me CH₂ CH₂ Ph (CH₂)₂ Me (S)- I-183 Me Me Me CH₂ CH₂ Ph C≡CCH₂ H racemic I-184 Me Me Me CH₂ CH₂ Ph C≡CCH₂ H (S)- I-185 Me Me Me CH₂ CH₂ Ph C≡CCH₂ Me racemic I-186 Me Me Me CH₂ CH₂ Ph C≡CCH₂ Me (S)- I-187 Me Me Me CH₂C(Me)₂ CH₂ Ph CH₂ H racemic I-188 Me Me Me CH₂C(Me)₂ CH₂ Ph CH₂ H (S)- I-189 Me Me Me CH₂C(Me)₂ CH₂ Ph — H racemic I-190 Me Me Me CH₂C(Me)₂ CH₂ Ph — H (S)- I-191 Me Me Me CH₂C(Me)₂ CH₂ Ph CH₂ Me racemic I-192 Me Me Me CH₂C(Me)₂ CH₂ Ph CH₂ Me (S)- I-193 Me Me Me CH₂C(Me)₂ CH₂ Ph C(Me)₂ H racemic I-194 Me Me Me CH₂C(Me)₂ CH₂ Ph C(Me)₂ H (S)- I-195 Me Me Me CH₂C(Me)₂ CH₂ Ph C(Me)₂ Me racemic I-196 Me Me Me CH₂C(Me)₂ CH₂ Ph C(Me)₂ Me (S)- I-197 Me Me Me CH₂C(Me)₂ CH₂ Ph (CH₂)₂ H racemic I-198 Me Me Me CH₂C(Me)₂ CH₂ Ph (CH₂)₂ H (S)- I-199 Me Me Me CH₂C(Me)₂ CH₂ Ph (CH₂)₂ Me racemic I-200 Me Me Me CH₂C(Me)₂ CH₂ Ph (CH₂)₂ Me (S)-

TABLE 5 (I)

Com- Con- pound figu- No. R¹ R² R³ L¹ L² R⁴ L³ R⁵ ration I-201 Me Me Me CH₂C(Me)₂ CH₂ Ph C≡CCH₂ H racemic I-202 Me Me Me CH₂C(Me)₂ CH₂ Ph C≡CCH₂ H (S)- I-203 Me Me Me CH₂C(Me)₂ CH₂ Ph C≡CCH₂ Me racemic I-204 Me Me Me CH₂C(Me)₂ CH₂ Ph C≡CCH₂ Me (S)- I-205 Me Me Me CH₂CH═CH CH₂ Ph CH₂ H racemic I-206 Me Me Me CH₂CH═CH CH₂ Ph CH₂ H (S)- I-207 Me Me Me CH₂CH═CH CH₂ Ph — H racemic I-208 Me Me Me CH₂CH═CH CH₂ Ph — H (S)- I-209 Me Me Me CH₂CH═CH CH₂ Ph CH₂ Me racemic I-210 Me Me Me CH₂CH═CH CH₂ Ph CH₂ Me (S)- I-211 Me Me Me CH₂CH═CH CH₂ Ph C(Me)₂ H racemic I-212 Me Me Me CH₂CH═CH CH₂ Ph C(Me)₂ H (S)- I-213 Me Me Me CH₂CH═CH CH₂ Ph C(Me)₂ Me racemic I-214 Me Me Me CH₂CH═CH CH₂ Ph C(Me)₂ Me (S)- I-215 Me Me Me CH₂CH═CH CH₂ Ph (CH₂)₂ H racemic I-216 Me Me Me CH₂CH═CH CH₂ Ph (CH₂)₂ H (S)- I-217 Me Me Me CH₂CH═CH CH₂ Ph (CH₂)₂ Me racemic I-218 Me Me Me CH₂CH═CH CH₂ Ph (CH₂)₂ Me (S)- I-219 Me Me Me CH₂CH═CH CH₂ Ph C≡CCH₂ H racemic I-220 Me Me Me CH₂CH═CH CH₂ Ph C≡CCH₂ H (S)- I-221 Me Me Me CH₂CH═CH CH₂ Ph C≡CCH₂ Me racemic I-222 Me Me Me CH₂CH═CH CH₂ Ph C≡CCH₂ Me (S)- I-223 Me Me Me CH₂C≡C CH₂ Ph CH₂ H racemic I-224 Me Me Me CH₂C≡C CH₂ Ph CH₂ H (S)- I-225 Me Me Me CH₂C≡C CH₂ Ph — H racemic I-226 Me Me Me CH₂C≡C CH₂ Ph — H (S)- I-227 Me Me Me CH₂C≡C CH₂ Ph CH₂ Me racemic I-228 Me Me Me CH₂C≡C CH₂ Ph CH₂ Me (S)- I-229 Me Me Me CH₂C≡C CH₂ Ph C(Me)₂ H racemic I-230 Me Me Me CH₂C≡C CH₂ Ph C(Me)₂ H (S)- I-231 Me Me Me CH₂C≡C CH₂ Ph C(Me)₂ Me racemic I-232 Me Me Me CH₂C≡C CH₂ Ph C(Me)₂ Me (S)- I-233 Me Me Me CH₂C≡C CH₂ Ph (CH₂)₂ H racemic I-234 Me Me Me CH₂C≡C CH₂ Ph (CH₂)₂ H (S)- I-235 Me Me Me CH₂C≡C CH₂ Ph (CH₂)₂ Me racemic I-236 Me Me Me CH₂C≡C CH₂ Ph (CH₂)₂ Me (S)- I-237 Me Me Me CH₂C≡C CH₂ Ph C≡CCH₂ H racemic I-238 Me Me Me CH₂C≡C CH₂ Ph C≡CCH₂ H (S)- I-239 Me Me Me CH₂C≡C CH₂ Ph C≡CCH₂ Me racemic I-240 Me Me Me CH₂C≡C CH₂ Ph C≡CCH₂ Me (S)- I-241 Me Me Me 1,2-Cyclo- CH₂ Ph CH₂ H racemic propylene I-242 Me Me Me 1,2-Cyclo- CH₂ Ph CH₂ H (S)- propylene I-243 Me Me Me 1,2-Cyclo- CH₂ Ph — H racemic propylene I-244 Me Me Me 1,2-Cyclo- CH₂ Ph — H (S)- propylene I-245 Me Me Me 1,2-Cyclo- CH₂ Ph CH₂ Me racemic propylene I-246 Me Me Me 1,2-Cyclo- CH₂ Ph CH₂ Me (S)- propylene I-247 Me Me Me 1,2-Cyclo- CH₂ Ph C(Me)₂ H racemic propylene I-248 Me Me Me 1,2-Cyclo- CH₂ Ph C(Me)₂ H (S)- propylene I-249 Me Me Me 1,2-Cyclo- CH₂ Ph C(Me)₂ Me racemic propylene I-250 Me Me Me 1,2-Cyclo- CH₂ Ph C(Me)₂ Me (S)- propylene

TABLE 6 (I)

Com- Con- pound figur- No. R¹ R² R³ L¹ L² R⁴ L³ R⁵ ation I-251 Me Me Me 1,2-Cyclo- CH₂ Ph (CH₂)₂ H racemic propylene I-252 Me Me Me 1,2-Cyclo- CH₂ Ph (CH₂)₂ H (S)- propylene I-253 Me Me Me 1,2-Cyclo- CH₂ Ph (CH₂)₂ Me racemic propylene I-254 Me Me Me 1,2-Cyclo- CH₂ Ph (CH₂)₂ Me (S)- propylene I-255 Me Me Me 1,2-Cyclo- CH₂ Ph C≡CCH₂ H racemic propylene I-256 Me Me Me 1,2-Cyclo- CH₂ Ph C≡CCH₂ H (S)- propylene I-257 Me Me Me 1,2-Cyclo- CH₂ Ph C≡CCH₂ Me racemic propylene I-258 Me Me Me 1,2-Cyclo- CH₂ Ph C≡CCH₂ Me (S)- propylene I-259 Me Me Me 5,5-Spiro- CH₂ Ph CH₂ H racemic [2.3]hexyl- ene I-260 Me Me Me 5,5-Spiro- CH₂ Ph CH₂ H (S)- [2.3]hexyl- ene I-261 Me Me Me 5,5-Spiro- CH₂ Ph — H racemic [2.3]hexyl- ene I-262 Me Me Me 5,5-Spiro- CH₂ Ph — H (S)- [2.3]hexyl- ene I-263 Me Me Me 5,5-Spiro- CH₂ Ph CH₂ Me racemic [2.3]hexyl- ene I-264 Me Me Me 5,5-Spiro- CH₂ Ph CH₂ Me (S)- [2.3]hexyl- ene I-265 Me Me Me 5,5-Spiro- CH₂ Ph C(Me)₂ H racemic [2.3]hexyl- ene I-266 Me Me Me 5,5-Spiro- CH₂ Ph C(Me)₂ H (S)- [2.3]hexyl- ene I-267 Me Me Me 5,5-Spiro- CH₂ Ph C(Me)₂ Me racemic [2.3]hexyl- ene I-268 Me Me Me 5,5-Spiro- CH₂ Ph C(Me)₂ Me (S)- [2.3]hexyl- ene I-269 Me Me Me 5,5-Spiro- CH₂ Ph (CH₂)₂ H racemic [2.3]hexyl- ene I-270 Me Me Me 5,5-Spiro- CH₂ Ph (CH₂)₂ H (S)- [2.3]hexyl- ene I-271 Me Me Me 5,5-Spiro- CH₂ Ph (CH₂)₂ Me racemic [2.3]hexyl- ene I-272 Me Me Me 5,5-Spiro- CH₂ Ph (CH₂)₂ Me (S)- [2.3]hexyl- ene I-273 Me Me Me 5,5-Spiro- CH₂ Ph C≡CCH₂ H racemic [2.3]hexyl- ene I-274 Me Me Me 5,5-Spiro- CH₂ Ph C≡CCH₂ H (S)- [2.3]hexyl- ene I-275 Me Me Me 5,5-Spiro- CH₂ Ph C≡CCH₂ Me racemic [2.3]hexyl- ene I-276 Me Me Me 5,5-Spiro- CH₂ Ph C≡CCH₂ Me (S)- [2.3]hexyl- ene I-277 Me Me Me 4,4-Cyclo- CH₂ Ph CH₂ H racemic pentenylene I-278 Me Me Me 4,4-Cyclo- CH₂ Ph CH₂ H (S)- pentenylene I-279 Me Me Me 4,4-Cyclo- CH₂ Ph — H racemic pentenylene I-280 Me Me Me 4,4-Cyclo- CH₂ Ph — H (S)- pentenylene I-281 Me Me Me 4,4-Cyclo- CH₂ Ph CH₂ Me racemic pentenylene I-282 Me Me Me 4,4-Cyclo- CH₂ Ph CH₂ Me (S)- pentenylene I-283 Me Me Me 4,4-Cyclo- CH₂ Ph C(Me)₂ H racemic pentenylene I-284 Me Me Me 4,4-Cyclo- CH₂ Ph C(Me)₂ H (S)- pentenylene I-285 Me Me Me 4,4-Cyclo- CH₂ Ph C(Me)₂ Me racemic pentenylene I-286 Me Me Me 4,4-Cyclo- CH₂ Ph C(Me)₂ Me (S)- pentenylene I-287 Me Me Me 4,4-Cyclo- CH₂ Ph (CH₂)₂ H racemic pentenylene I-288 Me Me Me 4,4-Cyclo- CH₂ Ph (CH₂)₂ H (S)- pentenylene I-289 Me Me Me 4,4-Cyclo- CH₂ Ph (CH₂)₂ Me racemic pentenylene I-290 Me Me Me 4,4-Cyclo- CH₂ Ph (CH₂)₂ Me (S)- pentenylene I-291 Me Me Me 4,4-Cyclo- CH₂ Ph C≡CCH₂ H racemic pentenylene I-292 Me Me Me 4,4-Cyclo- CH₂ Ph C≡CCH₂ H (S)- pentenylene I-293 Me Me Me 4,4-Cyclo- CH₂ Ph C≡CCH₂ Me racemic pentenylene I-294 Me Me Me 4,4-Cyclo- CH₂ Ph C≡CCH₂ Me (S)- pentenylene

TABLE 7 (I)

Com- Con- pound figur- No. R¹ R² R³ L¹ L² R⁴ L³ R⁵ ation I-295 Me Me Me 5,5-Spiro- NH Ph CH₂C(Me)₂ H racemic [2.3]hexyl- ene I-296 Me Me Me 5,5-Spiro- NH Ph CH₂C(Me)₂ H (R)- [2.3]hexyl- ene I-297 Me Me Me 5,5-Spiro- NH Ph CH₂C(Me)₂ Me racemic [2.3]hexyl- ene I-298 Me Me Me 5,5-Spiro- NH Ph CH₂C(Me)₂ Me (R)- [2.3]hexyl- ene I-299 Me Me Me 5,5-Spiro- NH Ph C(Me)₂CH₂ H racemic [2.3]hexyl- ene I-300 Me Me Me 5,5-Spiro- NH Ph C(Me)₂CH₂ H (+) [2.3]hexyl- ene I-301 Me Me Me 5,5-Spiro- NH Ph C(Me)₂CH₂ H (−) [2.3]hexyl- ene I-302 Me Me Me 5,5-Spiro- NH Ph C(Me)₂CH₂ Me racemic [2.3]hexyl- ene I-303 Me Me Me 5,5-Spiro- NH Ph C(Me)₂CH₂ Me (+) [2.3]hexyl- ene I-304 Me Me Me 5,5-Spiro- NH Ph C(Me)₂CH₂ Me (−) [2.3]hexyl- ene I-305 Me Me Me 4,4-Cyclo- NH Ph CH₂C(Me)₂ H racemic pentenylene I-306 Me Me Me 4,4-Cyclo- NH Ph CH₂C(Me)₂ H (R)- pentenylene I-307 Me Me Me 4,4-Cyclo- NH Ph CH₂C(Me)₂ Me racemic pentenylene I-308 Me Me Me 4,4-Cyclo- NH Ph CH₂C(Me)₂ Me (R)- pentenylene I-309 Me Me Me 4,4-Cyclo- NH Ph C(Me)₂CH₂ H racemic pentenylene I-310 Me Me Me 4,4-Cyclo- NH Ph C(Me)₂CH₂ H (+) pentenylene I-311 Me Me Me 4,4-Cyclo- NH Ph C(Me)₂CH₂ H (−) pentenylene I-312 Me Me Me 4,4-Cyclo- NH Ph C(Me)₂CH₂ Me racemic pentenylene I-313 Me Me Me 4,4-Cyclo- NH Ph C(Me)₂CH₂ Me (+) pentenylene I-314 Me Me Me 4,4-Cyclo- NH Ph C(Me)₂CH₂ Me (−) pentenylene I-315 Me Me Me 1,2-Cyclo- — Ph — H racemic propylene I-316 Me Me Me 1,2-Cyclo- — Ph — H (S)- propylene I-317 Me Me Me 1,2-Cyclo- — Ph — Me racemic propylene I-318 Me Me Me 1,2-Cyclo- — Ph — Me (S)- propylene I-319 Me Me Me 5,5-Spiro- — Ph — H racemic [2.3]hexyl- ene I-320 Me Me Me 5,5-Spiro- — Ph — H (S)- [2.3]hexyl- ene I-321 Me Me Me 5,5-Spiro- — Ph — Me racemic [2.3]hexyl- ene I-322 Me Me Me 5,5-Spiro- — Ph — Me (S)- [2.3]hexyl- ene I-323 Me Me Me 4,4-Cyclo- — Ph — H racemic pentenylene I-324 Me Me Me 4,4-Cyclo- — Ph — H (S)- pentenylene I-325 Me Me Me 4,4-Cyclo- Ph — Me racemic pentenylene I-326 Me Me Me 4,4-Cyclo- — Ph — Me (S)- pentenylene I-327 Me Me Me 1,2-Cyclo- — Ph CH₂ H racemic propylene I-328 Me Me Me 1,2-Cyclo- — Ph CH₂ H (S)- propylene I-329 Me Me Me 1,2-Cyclo- — Ph CH₂ Me racemic propylene I-330 Me Me Me 1,2-Cyclo- — Ph CH₂ Me (S)- propylene I-331 Me Me Me 1,2-Cyclo- — Ph (CH₂)₂ H racemic propylene I-332 Me Me Me 1,2-Cyclo- — Ph (CH₂)₂ H (S)- propylene I-333 Me Me Me 1,2-Cyclo- — Ph (CH₂)₂ Me racemic propylene I-334 Me Me Me 1,2-Cyclo- — Ph (CH₂)₂ Me (S)- propylene I-335 Me Me Me 5,5-Spiro- — Ph CH₂ H racemic [2.3]hexyl- ene I-336 Me Me Me 5,5-Spiro- — Ph CH₂ H (S)- [2.3]hexyl- ene I-337 Me Me Me 5,5-Spiro- — Ph CH₂ Me racemic [2.3]hexyl- ene I-338 Me Me Me 5,5-Spiro- — Ph CH₂ Me (S)- [2.3]hexyl- ene I-339 Me Me Me 5,5-Spiro- — Ph (CH₂)₂ H racemic [2.3]hexyl- ene I-340 Me Me Me 5,5-Spiro- — Ph (CH₂)₂ H (S)- [2.3]hexyl- ene I-341 Me Me Me 5,5-Spiro- — Ph (CH₂)₂ Me racemic [2.3]hexyl- ene I-342 Me Me Me 5,5-Spiro- — Ph (CH₂)₂ Me (S)- [2.3]hexyl- ene I-343 Me Me Me 4,4-Cyclo- — Ph CH₂ H racemic pentenylene I-344 Me Me Me 4,4-Cyclo- — Ph CH₂ H (S)- pentenylene I-345 Me Me Me 4,4-Cyclo- — Ph CH₂ Me racemic pentenylene

TABLE 8 (I)

Com- Con- pound figur- No. R¹ R² R³ L¹ L² R⁴ L³ R⁵ ation I-346 Me Me Me 4,4-Cyclo- — Ph CH₂ Me (S)- pentenylene I-347 Me Me Me 4,4-Cyclo- — Ph (CH₂)₂ H racemic pentenylene I-348 Me Me Me 4,4-Cyclo- — Ph (CH₂)₂ H (S)- pentenylene I-349 Me Me Me 4,4-Cyclo- — Ph (CH₂)₂ Me racemic pentenylene I-350 Me Me Me 4,4-Cyclo- — Ph (CH₂)₂ Me (S)- pentenylene

TABLE 9 (II)

Compound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration II-1 Me Me Me O Ph CH₂ H racemic II-2 Me Me Me O Ph CH₂ H (S)- II-3 Me Et Me O Ph CH₂ H racemic II-4 Me Et Me O Ph CH₂ H (S)- II-5 Me Me Me O Ph CH₂ Me racemic II-6 Me Me Me O Ph CH₂ Me (S)- II-7 Me Et Me O Ph CH₂ Me racemic II-8 Me Et Me O Ph CH₂ Me (S)- II-9 Me Me Me O Ph CH₂ CHF₂ racemic II-10 Me Me Me O Ph CH₂ CHF₂ (S)- II-11 Me Et Me O Ph CH₂ CHF₂ racemic II-12 Me Et Me O Ph CH₂ CHF₂ (S)- II-13 Me Me Me O Ph CH₂ Et racemic II-14 Me Me Me O Ph CH₂ Et (S)- II-15 Me Et Me O Ph CH₂ Et racemic II-16 Me Et Me O Ph CH₂ Et (S)- II-17 Me Me Me O Ph CH₂ iPr racemic II-18 Me Me Me O Ph CH₂ iPr (S)- II-19 Me Et Me O Ph CH₂ iPr racemic II-20 Me Et Me O Ph CH₂ iPr (S)- II-21 Me Me Me O Ph CH₂ cPr racemic II-22 Me Me Me O Ph CH₂ cPr (S)- II-23 Me Et Me O Ph CH₂ cPr racemic II-24 Me Et Me O Ph CH₂ cPr (S)- II-25 Me Me Me O Ph CH₂ Ph racemic II-26 Me Me Me O Ph CH₂ Ph (S)- II-27 Me Et Me O Ph CH₂ Ph racemic II-28 Me Et Me O Ph CH₂ Ph (S)- II-29 Me Me Me O Ph C(Me)₂ H racemic II-30 Me Me Me O Ph C(Me)₂ H (S)- II-31 Me Et Me O Ph C(Me)₂ H racemic II-32 Me Et Me O Ph C(Me)₂ H (S)- II-33 Me Me Me O Ph C(Me)₂ Me racemic II-34 Me Me Me O Ph C(Me)₂ Me (S)- II-35 Me Et Me O Ph C(Me)₂ Me racemic II-36 Me Et Me O Ph C(Me)₂ Me (S)- II-37 Me Me Me O Ph C(Me)₂ CHF₂ racemic II-38 Me Me Me O Ph C(Me)₂ CHF₂ (S)- II-39 Me Et Me O Ph C(Me)₂ CHF₂ racemic II-40 Me Et Me O Ph C(Me)₂ CHF₂ (S)- II-41 Me Me Me O Ph C(Me)₂ Et racemic II-42 Me Me Me O Ph C(Me)₂ Et (S)- II-43 Me Et Me O Ph C(Me)₂ Et racemic II-44 Me Et Me O Ph C(Me)₂ Et (S)- II-45 Me Me Me O Ph C(Me)₂ iPr racemic II-46 Me Me Me O Ph C(Me)₂ iPr (S)- II-47 Me Et Me O Ph C(Me)₂ iPr racemic II-48 Me Et Me O Ph C(Me)₂ iPr (S)- II-49 Me Me Me O Ph C(Me)₂ cPr racemic II-50 Me Me Me O Ph C(Me)₂ cPr (S)-

TABLE 10 (II)

Compound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration II-51 Me Et Me O Ph C(Me)₂ cPr racemic II-52 Me Et Me O Ph C(Me)₂ cPr (S)- II-53 Me Me Me O Ph C(Me)₂ Ph racemic II-54 Me Me Me O Ph C(Me)₂ Ph (S)- II-55 Me Et Me O Ph C(Me)₂ Ph racemic II-56 Me Et Me O Ph C(Me)₂ Ph (S)- II-57 Me Me Me O Ph (CH₂)₂ H racemic II-58 Me Me Me O Ph (CH₂)₂ H (R)- II-59 Me Et Me O Ph (CH₂)₂ H racemic II-60 Me Et Me O Ph (CH₂)₂ H (R)- II-61 Me Me Me O Ph (CH₂)₂ Me racemic II-62 Me Me Me O Ph (CH₂)₂ Me (R)- II-63 Me Et Me O Ph (CH₂)₂ Me racemic II-64 Me Et Me O Ph (CH₂)₂ Me (R)- II-65 Me Me Me O Ph (CH₂)₂ CHF₂ racemic II-66 Me Me Me O Ph (CH₂)₂ CHF₂ (R)- II-67 Me Et Me O Ph (CH₂)₂ CHF₂ racemic II-68 Me Et Me O Ph (CH₂)₂ CHF₂ (R)- II-69 Me Me Me O Ph (CH₂)₂ Et racemic II-70 Me Me Me O Ph (CH₂)₂ Et (R)- II-71 Me Et Me O Ph (CH₂)₂ Et racemic II-72 Me Et Me O Ph (CH₂)₂ Et (R)- II-73 Me Me Me O Ph (CH₂)₂ iPr racemic II-74 Me Me Me O Ph (CH₂)₂ iPr (R)- II-75 Me Et Me O Ph (CH₂)₂ iPr racemic II-76 Me Et Me O Ph (CH₂)₂ iPr (R)- II-77 Me Me Me O Ph (CH₂)₂ cPr racemic II-78 Me Me Me O Ph (CH₂)₂ cPr (R)- II-79 Me Et Me O Ph (CH₂)₂ cPr racemic II-80 Me Et Me O Ph (CH₂)₂ cPr (R)- II-81 Me Me Me O Ph (CH₂)₂ Ph racemic II-82 Me Me Me O Ph (CH₂)₂ Ph (R)- II-83 Me Et Me O Ph (CH₂)₂ Ph racemic II-84 Me Et Me O Ph (CH₂)₂ Ph (R)- II-85 Me Me Me O Ph CH₂C(Me)₂ H racemic II-86 Me Me Me O Ph CH₂C(Me)₂ H (R)- II-87 Me Et Me O Ph CH₂C(Me)₂ H racemic II-88 Me Et Me O Ph CH₂C(Me)₂ H (R)- II-89 Me Me Me O Ph CH₂C(Me)₂ Me racemic II-90 Me Me Me O Ph CH₂C(Me)₂ Me (R)- II-91 Me Et Me O Ph CH₂C(Me)₂ Me racemic II-92 Me Et Me O Ph CH₂C(Me)₂ Me (R)- II-93 Me Me Me O Ph CH₂C(Me)₂ CHF₂ racemic II-94 Me Me Me O Ph CH₂C(Me)₂ CHF₂ (R)- II-95 Me Et Me O Ph CH₂C(Me)₂ CHF₂ racemic II-96 Me Et Me O Ph CH₂C(Me)₂ CHF₂ (R)- II-97 Me Me Me O Ph CH₂C(Me)₂ Et racemic II-98 Me Me Me O Ph CH₂C(Me)₂ Et (R)- II-99 Me Et Me O Ph CH₂C(Me)₂ Et racemic II-100 Me Et Me O Ph CH₂C(Me)₂ Et (R)-

TABLE 11 (II)

Compound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration II-101 Me Me Me O Ph CH₂C(Me)₂ iPr racemic II-102 Me Me Me O Ph CH₂C(Me)₂ iPr (R)- II-103 Me Et Me O Ph CH₂C(Me)₂ iPr racemic II-104 Me Et Me O Ph CH₂C(Me)₂ iPr (R)- II-105 Me Me Me O Ph CH₂C(Me)₂ cPr racemic II-106 Me Me Me O Ph CH₂C(Me)₂ cPr (R)- II-107 Me Et Me O Ph CH₂C(Me)₂ cPr racemic II-108 Me Et Me O Ph CH₂C(Me)₂ cPr (R)- II-109 Me Me Me O Ph CH₂C(Me)₂ Ph racemic II-110 Me Me Me O Ph CH₂C(Me)₂ Ph (R)- II-111 Me Et Me O Ph CH₂C(Me)₂ Ph racemic II-112 Me Et Me O Ph CH₂C(Me)₂ Ph (R)- II-113 Me Me Me NH Ph CH₂ H racemic II-114 Me Me Me NH Ph CH₂ H (S)- II-115 Me Et Me NH Ph CH₂ H racemic II-116 Me Et Me NH Ph CH₂ H (S)- II-117 Me Me Me N(Me) Ph CH₂ H racemic II-118 Me Me Me N(Me) Ph CH₂ H (S)- II-119 Me Et Me N(Me) Ph CH₂ H racemic II-120 Me Et Me N(Me) Ph CH₂ H (S)- II-121 Me Me Me NH Ph CH₂ Me racemic II-122 Me Me Me NH Ph CH₂ Me (S)- II-123 Me Et Me NH Ph CH₂ Me racemic II-124 Me Et Me NH Ph CH₂ Me (S)- II-125 Me Me Me N(Me) Ph CH₂ Me racemic II-126 Me Me Me N(Me) Ph CH₂ Me (S)- II-127 Me Et Me N(Me) Ph CH₂ Me racemic II-128 Me Et Me N(Me) Ph CH₂ Me (S)- II-129 Me Me Me NH Ph CH₂ CHF₂ racemic II-130 Me Me Me NH Ph CH₂ CHF₂ (S)- II-131 Me Et Me NH Ph CH₂ CHF₂ racemic II-132 Me Et Me NH Ph CH₂ CHF₂ (S)- II-133 Me Me Me N(Me) Ph CH₂ CHF₂ racemic II-134 Me Me Me N(Me) Ph CH₂ CHF₂ (S)- II-135 Me Et Me N(Me) Ph CH₂ CHF₂ racemic II-136 Me Et Me N(Me) Ph CH₂ CHF₂ (S)- II-137 Me Me Me NH Ph CH₂ Et racemic II-138 Me Me Me NH Ph CH₂ Et (S)- II-139 Me Et Me NH Ph CH₂ Et racemic II-140 Me Et Me NH Ph CH₂ Et (S)- II-141 Me Me Me N(Me) Ph CH₂ Et racemic II-142 Me Me Me N(Me) Ph CH₂ Et (S)- II-143 Me Et Me N(Me) Ph CH₂ Et racemic II-144 Me Et Me N(Me) Ph CH₂ Et (S)- II-145 Me Me Me NH Ph CH₂ iPr racemic II-146 Me Me Me NH Ph CH₂ iPr (S)- II-147 Me Et Me NH Ph CH₂ iPr racemic II-148 Me Et Me NH Ph CH₂ iPr (S)- II-149 Me Me Me N(Me) Ph CH₂ iPr racemic II-150 Me Me Me N(Me) Ph CH₂ iPr (S)-

TABLE 12 (II)

Compound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration II-151 Me Et Me N(Me) Ph CH₂ iPr racemic II-152 Me Et Me N(Me) Ph CH₂ iPr (S)- II-153 Me Me Me NH Ph CH₂ cPr racemic II-154 Me Me Me NH Ph CH₂ cPr (S)- II-155 Me Et Me NH Ph CH₂ cPr racemic II-156 Me Et Me NH Ph CH₂ cPr (S)- II-157 Me Me Me N(Me) Ph CH₂ cPr racemic II-158 Me Me Me N(Me) Ph CH₂ cPr (S)- II-159 Me Et Me N(Me) Ph CH₂ cPr racemic II-160 Me Et Me N(Me) Ph CH₂ cPr (S)- II-161 Me Me Me NH Ph CH₂ Ph racemic II-162 Me Me Me NH Ph CH₂ Ph (S)- II-163 Me Et Me NH Ph CH₂ Ph racemic II-164 Me Et Me NH Ph CH₂ Ph (S)- II-165 Me Me Me N(Me) Ph CH₂ Ph racemic II-166 Me Me Me N(Me) Ph CH₂ Ph (S)- II-167 Me Et Me N(Me) Ph CH₂ Ph racemic II-168 Me Et Me N(Me) Ph CH₂ Ph (S)- II-169 Me Me Me NH Ph C(Me)₂ H racemic II-170 Me Me Me NH Ph C(Me)₂ H (S)- II-171 Me Et Me NH Ph C(Me)₂ H racemic II-172 Me Et Me NH Ph C(Me)₂ H (S)- II-173 Me Me Me N(Me) Ph C(Me)₂ H racemic II-174 Me Me Me N(Me) Ph C(Me)₂ H (S)- II-175 Me Et Me N(Me) Ph C(Me)₂ H racemic II-176 Me Et Me N(Me) Ph C(Me)₂ H (S)- II-177 Me Me Me NH Ph C(Me)₂ Me racemic II-178 Me Me Me NH Ph C(Me)₂ Me (S)- II-179 Me Et Me NH Ph C(Me)₂ Me racemic II-180 Me Et Me NH Ph C(Me)₂ Me (S)- II-181 Me Me Me N(Me) Ph C(Me)₂ Me racemic II-182 Me Me Me N(Me) Ph C(Me)₂ Me (S)- II-183 Me Et Me N(Me) Ph C(Me)₂ Me racemic II-184 Me Et Me N(Me) Ph C(Me)₂ Me (S)- II-185 Me Me Me NH Ph C(Me)₂ CHF₂ racemic II-186 Me Me Me NH Ph C(Me)₂ CHF₂ (S)- II-187 Me Et Me NH Ph C(Me)₂ CHF₂ racemic II-188 Me Et Me NH Ph C(Me)₂ CHF₂ (S)- II-189 Me Me Me N(Me) Ph C(Me)₂ CHF₂ racemic II-190 Me Me Me N(Me) Ph C(Me)₂ CHF₂ (S)- II-191 Me Et Me N(Me) Ph C(Me)₂ CHF₂ racemic II-192 Me Et Me N(Me) Ph C(Me)₂ CHF₂ (S)- II-193 Me Me Me NH Ph C(Me)₂ Et racemic II-194 Me Me Me NH Ph C(Me)₂ Et (S)- II-195 Me Et Me NH Ph C(Me)₂ Et racemic II-196 Me Et Me NH Ph C(Me)₂ Et (S)- II-197 Me Me Me N(Me) Ph C(Me)₂ Et racemic II-198 Me Me Me N(Me) Ph C(Me)₂ Et (S)- II-199 Me Et Me N(Me) Ph C(Me)₂ Et racemic II-200 Me Et Me N(Me) Ph C(Me)₂ Et (S)-

TABLE 13 (II)

Compound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration II-201 Me Me Me NH Ph C(Me)₂ iPr racemic II-202 Me Me Me NH Ph C(Me)₂ iPr (S)- II-203 Me Et Me NH Ph C(Me)₂ iPr racemic II-204 Me Et Me NH Ph C(Me)₂ iPr (S)- II-205 Me Me Me N(Me) Ph C(Me)₂ iPr racemic II-206 Me Me Me N(Me) Ph C(Me)₂ iPr (S)- II-207 Me Et Me N(Me) Ph C(Me)₂ iPr racemic II-208 Me Et Me N(Me) Ph C(Me)₂ iPr (S)- II-209 Me Me Me NH Ph C(Me)₂ cPr racemic II-210 Me Me Me NH Ph C(Me)₂ cPr (S)- II-211 Me Et Me NH Ph C(Me)₂ cPr racemic II-212 Me Et Me NH Ph C(Me)₂ cPr (S)- II-213 Me Me Me N(Me) Ph C(Me)₂ cPr racemic II-214 Me Me Me N(Me) Ph C(Me)₂ cPr (S)- II-215 Me Et Me N(Me) Ph C(Me)₂ cPr racemic II-216 Me Et Me N(Me) Ph C(Me)₂ cPr (S)- II-217 Me Me Me NH Ph C(Me)₂ Ph racemic II-218 Me Me Me NH Ph C(Me)₂ Ph (S)- II-219 Me Et Me NH Ph C(Me)₂ Ph racemic II-220 Me Et Me NH Ph C(Me)₂ Ph (S)- II-221 Me Me Me N(Me) Ph C(Me)₂ Ph racemic II-222 Me Me Me N(Me) Ph C(Me)₂ Ph (S)- II-223 Me Et Me N(Me) Ph C(Me)₂ Ph racemic II-224 Me Et Me N(Me) Ph C(Me)₂ Ph (S)- II-225 Me Me Me NH Ph (CH₂)₂ H racemic II-226 Me Me Me NH Ph (CH₂)₂ H (R)- II-227 Me Et Me NH Ph (CH₂)₂ H racemic II-228 Me Et Me NH Ph (CH₂)₂ H (R)- II-229 Me Me Me N(Me) Ph (CH₂)₂ H racemic II-230 Me Me Me N(Me) Ph (CH₂)₂ H (R)- II-231 Me Et Me N(Me) Ph (CH₂)₂ H racemic II-232 Me Et Me N(Me) Ph (CH₂)₂ H (R)- II-233 Me Me Me NH Ph (CH₂)₂ Me racemic II-234 Me Me Me NH Ph (CH₂)₂ Me (R)- II-235 Me Et Me NH Ph (CH₂)₂ Me racemic II-236 Me Et Me NH Ph (CH₂)₂ Me (R)- II-237 Me Me Me N(Me) Ph (CH₂)₂ Me racemic II-238 Me Me Me N(Me) Ph (CH₂)₂ Me (R)- II-239 Me Et Me N(Me) Ph (CH₂)₂ Me racemic II-240 Me Et Me N(Me) Ph (CH₂)₂ Me (R)- II-241 Me Me Me NH Ph (CH₂)₂ CHF₂ racemic II-242 Me Me Me NH Ph (CH₂)₂ CHF₂ (R)- II-243 Me Et Me NH Ph (CH₂)₂ CHF₂ racemic II-244 Me Et Me NH Ph (CH₂)₂ CHF₂ (R)- II-245 Me Me Me N(Me) Ph (CH₂)₂ CHF₂ racemic II-246 Me Me Me N(Me) Ph (CH₂)₂ CHF₂ (R)- II-247 Me Et Me N(Me) Ph (CH₂)₂ CHF₂ racemic II-248 Me Et Me N(Me) Ph (CH₂)₂ CHF₂ (R)- II-249 Me Me Me NH Ph (CH₂)₂ Et racemic II-250 Me Me Me NH Ph (CH₂)₂ Et (R)-

TABLE 14 (II)

Compound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration II-251 Me Et Me NH Ph (CH₂)₂ Et racemic II-252 Me Et Me NH Ph (CH₂)₂ Et (R)- II-253 Me Me Me N(Me) Ph (CH₂)₂ Et racemic II-254 Me Me Me N(Me) Ph (CH₂)₂ Et (R)- II-255 Me Et Me N(Me) Ph (CH₂)₂ Et racemic II-256 Me Et Me N(Me) Ph (CH₂)₂ Et (R)- II-257 Me Me Me NH Ph (CH₂)₂ iPr racemic II-258 Me Me Me NH Ph (CH₂)₂ iPr (R)- II-259 Me Et Me NH Ph (CH₂)₂ iPr racemic II-260 Me Et Me NH Ph (CH₂)₂ iPr (R)- II-261 Me Me Me N(Me) Ph (CH₂)₂ iPr racemic II-262 Me Me Me N(Me) Ph (CH₂)₂ iPr (R)- II-263 Me Et Me N(Me) Ph (CH₂)₂ iPr racemic II-264 Me Et Me N(Me) Ph (CH₂)₂ iPr (R)- II-265 Me Me Me NH Ph (CH₂)₂ cPr racemic II-266 Me Me Me NH Ph (CH₂)₂ cPr (R)- II-267 Me Et Me NH Ph (CH₂)₂ cPr racemic II-268 Me Et Me NH Ph (CH₂)₂ cPr (R)- II-269 Me Me Me N(Me) Ph (CH₂)₂ cPr racemic II-270 Me Me Me N(Me) Ph (CH₂)₂ cPr (R)- II-271 Me Et Me N(Me) Ph (CH₂)₂ cPr racemic II-272 Me Et Me N(Me) Ph (CH₂)₂ cPr (R)- II-273 Me Me Me NH Ph (CH₂)₂ Ph racemic II-274 Me Me Me NH Ph (CH₂)₂ Ph (R)- II-275 Me Et Me NH Ph (CH₂)₂ Ph racemic II-276 Me Et Me NH Ph (CH₂)₂ Ph (R)- II-277 Me Me Me N(Me) Ph (CH₂)₂ Ph racemic II-278 Me Me Me N(Me) Ph (CH₂)₂ Ph (R)- II-279 Me Et Me N(Me) Ph (CH₂)₂ Ph racemic II-280 Me Et Me N(Me) Ph (CH₂)₂ Ph (R)- II-281 Me Me Me NH Ph (CH₂)₃ H racemic II-282 Me Me Me NH Ph (CH₂)₃ H (R)- II-283 Me Et Me NH Ph (CH₂)₃ H racemic II-284 Me Et Me NH Ph (CH₂)₃ H (R)- II-285 Me Me Me N(Me) Ph (CH₂)₃ H racemic II-286 Me Me Me N(Me) Ph (CH₂)₃ H (R)- II-287 Me Et Me N(Me) Ph (CH₂)₃ H racemic II-288 Me Et Me N(Me) Ph (CH₂)₃ H (R)- II-289 Me Me Me NH Ph (CH₂)₄ H racemic II-290 Me Me Me NH Ph (CH₂)₄ H (R)- II-291 Me Et Me NH Ph (CH₂)₄ H racemic II-292 Me Et Me NH Ph (CH₂)₄ H (R)- II-293 Me Me Me N(Me) Ph (CH₂)₄ H racemic II-294 Me Me Me N(Me) Ph (CH₂)₄ H (R)- II-295 Me Et Me N(Me) Ph (CH₂)₄ H racemic II-296 Me Et Me N(Me) Ph (CH₂)₄ H (R)- II-297 Me Me Me NH Ph CH₂C(Me)₂ H racemic II-298 Me Me Me NH Ph CH₂C(Me)₂ H (R)- II-299 Me Et Me NH Ph CH₂C(Me)₂ H racemic II-300 Me Et Me NH Ph CH₂C(Me)₂ H (R)-

TABLE 15 (II)

Compound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration II-301 Me Me Me N(Me) Ph CH₂C(Me)₂ H racemic II-302 Me Me Me N(Me) Ph CH₂C(Me)₂ H (R)- II-303 Me Et Me N(Me) Ph CH₂C(Me)₂ H racemic II-304 Me Et Me N(Me) Ph CH₂C(Me)₂ H (R)- II-305 Me Me Me NH Ph CH₂C(Me)₂ Me racemic II-306 Me Me Me NH Ph CH₂C(Me)₂ Me (R)- II-307 Me Et Me NH Ph CH₂C(Me)₂ Me racemic II-308 Me Et Me NH Ph CH₂C(Me)₂ Me (R)- II-309 Me Me Me N(Me) Ph CH₂C(Me)₂ Me racemic II-310 Me Me Me N(Me) Ph CH₂C(Me)₂ Me (R)- II-311 Me Et Me N(Me) Ph CH₂C(Me)₂ Me racemic II-312 Me Et Me N(Me) Ph CH₂C(Me)₂ Me (R)- II-313 Me Me Me NH Ph CH₂C(Me)₂ CHF₂ racemic II-314 Me Me Me NH Ph CH₂C(Me)₂ CHF₂ (R)- II-315 Me Et Me NH Ph CH₂C(Me)₂ CHF₂ racemic II-316 Me Et Me NH Ph CH₂C(Me)₂ CHF₂ (R)- II-317 Me Me Me N(Me) Ph CH₂C(Me)₂ CHF₂ racemic II-318 Me Me Me N(Me) Ph CH₂C(Me)₂ CHF₂ (R)- II-319 Me Et Me N(Me) Ph CH₂C(Me)₂ CHF₂ racemic II-320 Me Et Me N(Me) Ph CH₂C(Me)₂ CHF₂ (R)- II-321 Me Me Me NH Ph CH₂C(Me)₂ Et racemic II-322 Me Me Me NH Ph CH₂C(Me)₂ Et (R)- II-323 Me Et Me NH Ph CH₂C(Me)₂ Et racemic II-324 Me Et Me NH Ph CH₂C(Me)₂ Et (R)- II-325 Me Me Me N(Me) Ph CH₂C(Me)₂ Et racemic II-326 Me Me Me N(Me) Ph CH₂C(Me)₂ Et (R)- II-327 Me Et Me N(Me) Ph CH₂C(Me)₂ Et racemic II-328 Me Et Me N(Me) Ph CH₂C(Me)₂ Et (R)- II-329 Me Me Me NH Ph CH₂C(Me)₂ iPr racemic II-330 Me Me Me NH Ph CH₂C(Me)₂ iPr (R)- II-331 Me Et Me NH Ph CH₂C(Me)₂ iPr racemic II-332 Me Et Me NH Ph CH₂C(Me)₂ iPr (R)- II-333 Me Me Me N(Me) Ph CH₂C(Me)₂ iPr racemic II-334 Me Me Me N(Me) Ph CH₂C(Me)₂ iPr (R)- II-335 Me Et Me N(Me) Ph CH₂C(Me)₂ iPr racemic II-336 Me Et Me N(Me) Ph CH₂C(Me)₂ iPr (R)- II-337 Me Me Me NH Ph CH₂C(Me)₂ cPr racemic II-338 Me Me Me NH Ph CH₂C(Me)₂ cPr (R)- II-339 Me Et Me NH Ph CH₂C(Me)₂ cPr racemic II-340 Me Et Me NH Ph CH₂C(Me)₂ cPr (R)- II-341 Me Me Me N(Me) Ph CH₂C(Me)₂ cPr racemic II-342 Me Me Me N(Me) Ph CH₂C(Me)₂ cPr (R)- II-343 Me Et Me N(Me) Ph CH₂C(Me)₂ cPr racemic II-344 Me Et Me N(Me) Ph CH₂C(Me)₂ cPr (R)- II-345 Me Me Me NH Ph CH₂C(Me)₂ Ph racemic II-346 Me Me Me NH Ph CH₂C(Me)₂ Ph (R)- II-347 Me Et Me NH Ph CH₂C(Me)₂ Ph racemic II-348 Me Et Me NH Ph CH₂C(Me)₂ Ph (R)- II-349 Me Me Me N(Me) Ph CH₂C(Me)₂ Ph racemic II-350 Me Me Me N(Me) Ph CH₂C(Me)₂ Ph (R)-

TABLE 16 (II)

Compound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration II-351 Me Et Me N(Me) Ph CH₂C(Me)₂ Ph racemic II-352 Me Et Me N(Me) Ph CH₂C(Me)₂ Ph (R)- II-353 Me Me Me NH Ph C(Me)₂CH₂ H racemic II-354 Me Me Me NH Ph C(Me)₂CH₂ H (S)- II-355 Me Et Me NH Ph C(Me)₂CH₂ H racemic II-356 Me Et Me NH Ph C(Me)₂CH₂ H (S)- II-357 Me Me Me N(Me) Ph C(Me)₂CH₂ H racemic II-358 Me Me Me N(Me) Ph C(Me)₂CH₂ H (S)- II-359 Me Et Me N(Me) Ph C(Me)₂CH₂ H racemic II-360 Me Et Me N(Me) Ph C(Me)₂CH₂ H (S)- II-361 Me Me Me NH Ph CF₂CH₂ H racemic II-362 Me Me Me NH Ph CF₂CH₂ H (S)- II-363 Me Et Me NH Ph CF₂CH₂ H racemic II-364 Me Et Me NH Ph CF₂CH₂ H (S)- II-365 Me Me Me N(Me) Ph CF₂CH₂ H racemic II-366 Me Me Me N(Me) Ph CF₂CH₂ H (S)- II-367 Me Et Me N(Me) Ph CF₂CH₂ H racemic II-368 Me Et Me N(Me) Ph CF₂CH₂ H (S)- II-369 Me Me Me NH Ph CH═CHCH₂ H racemic II-370 Me Me Me NH Ph CH═CHCH₂ H (S)- II-371 Me Et Me NH Ph CH═CHCH₂ H racemic II-372 Me Et Me NH Ph CH═CHCH₂ H (S)- II-373 Me Me Me N(Me) Ph CH═CHCH₂ H racemic II-374 Me Me Me N(Me) Ph CH═CHCH₂ H (S)- II-375 Me Et Me N(Me) Ph CH═CHCH₂ H racemic II-376 Me Et Me N(Me) Ph CH═CHCH₂ H (S)- II-377 Me Me Me NH Ph C≡CCH₂ H racemic II-378 Me Me Me NH Ph C≡CCH₂ H (S)- II-379 Me Et Me NH Ph C≡CCH₂ H racemic II-380 Me Et Me NH Ph C≡CCH₂ H (S)- II-381 Me Me Me N(Me) Ph C≡CCH₂ H racemic II-382 Me Me Me N(Me) Ph C≡CCH₂ H (S)- II-383 Me Et Me N(Me) Ph C≡CCH₂ H racemic II-384 Me Et Me N(Me) Ph C≡CCH₂ H (S)- II-385 Me Me Me NH Ph 1,1-Cyclo- H racemic propylene II-386 Me Me Me NH Ph 1,1-Cyclo- H (S)- propylene II-387 Me Et Me NH Ph 1,1-Cyclo- H racemic propylene II-388 Me Et Me NH Ph 1,1-Cyclo- H (S)- propylene II-389 Me Me Me N(Me) Ph 1,1-Cyclo- H racemic propylene II-390 Me Me Me N(Me) Ph 1,1-Cyclo- H (S)- propylene II-391 Me Et Me N(Me) Ph 1,1-Cyclo- H racemic propylene II-392 Me Et Me N(Me) Ph 1,1-Cyclo- H (S)- propylene II-393 Me Me Me NH Ph 1,2-Cyclo- H racemic propynylene II-394 Me Me Me NH Ph 1,2-Cyclo- H (S)- propynylene II-395 Me Et Me NH Ph 1,2-Cyclo- H racemic propynylene II-396 Me Et Me NH Ph 1,2-Cyclo- H (S)- propynylene II-397 Me Me Me N(Me) Ph 1,2-Cyclo- H racemic propynylene II-398 Me Me Me N(Me) Ph 1,2-Cyclo- H (S)- propynylene II-399 Me Et Me N(Me) Ph 1,2-Cyclo- H racemic propynylene II-400 Me Et Me N(Me) Ph 1,2-Cyclo- H (S)- propynylene

TABLE 17 (II)

Compound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration II-401 Me Me Me NH Ph C(═O) H racemic II-402 Me Me Me NH Ph C(═O) H (S)- II-403 Me Et Me NH Ph C(═O) H racemic II-404 Me Et Me NH Ph C(═O) H (S)- II-405 Me Me Me N(Me) Ph C(═O) H racemic II-406 Me Me Me N(Me) Ph C(═O) H (S)- II-407 Me Et Me N(Me) Ph C(═O) H racemic II-408 Me Et Me N(Me) Ph C(═O) H (S)- II-409 Me Me Me NH Ph C(═O) Bn racemic II-410 Me Me Me NH Ph C(═O) Bn (S)- II-411 Me Et Me NH Ph C(═O) Bn racemic II-412 Me Et Me NH Ph C(═O) Bn (S)- II-413 Me Me Me N(Me) Ph C(═O) Bn racemic II-414 Me Me Me N(Me) Ph C(═O) Bn (S)- II-415 Me Et Me N(Me) Ph C(═O) Bn racemic II-416 Me Et Me N(Me) Ph C(═O) Bn (S)- II-417 Me Me Me NH Ph C(═O) Me racemic II-418 Me Me Me NH Ph C(═O) Me (S)- II-419 Me Et Me NH Ph C(═O) Me racemic II-420 Me Et Me NH Ph C(═O) Me (S)- II-421 Me Me Me N(Me) Ph C(═O) Me racemic II-422 Me Me Me N(Me) Ph C(═O) Me (S)- II-423 Me Et Me N(Me) Ph C(═O) Me racemic II-424 Me Et Me N(Me) Ph C(═O) Me (S)- II-425 Me Me Me NH H CH₂ H II-426 Me Et Me NH H CH₂ H II-427 Me Me Me N(Me) H CH₂ H II-428 Me Et Me N(Me) H CH₂ H II-429 Me Me Me NH H CH(Me) H II-430 Me Et Me NH H CH(Me) H II-431 Me Me Me N(Me) H CH(Me) H II-432 Me Et Me N(Me) H CH(Me) H II-433 Me Me Me NH H CH(iPr) H II-434 Me Et Me NH H CH(iPr) H II-435 Me Me Me N(Me) H CH(iPr) H II-436 Me Et Me N(Me) H CH(iPr) H II-437 Me Me Me NH H CH(Ph) H II-438 Me Et Me NH H CH(Ph) H II-439 Me Me Me N(Me) H CH(Ph) H II-440 Me Et Me N(Me) H CH(Ph) H II-441 Me Me Me NH Me CH₂ H racemic II-442 Me Me Me NH Me CH₂ H (S)- II-443 Me Et Me NH Me CH₂ H racemic II-444 Me Et Me NH Me CH₂ H (S)- II-445 Me Me Me N(Me) Me CH₂ H racemic II-446 Me Me Me N(Me) Me CH₂ H (S)- II-447 Me Et Me N(Me) Me CH₂ H racemic II-448 Me Et Me N(Me) Me CH₂ H (S)- II-449 Me Me Me NH iPr CH₂ H racemic II-450 Me Me Me NH iPr CH₂ H (S)-

TABLE 18 (II)

Compound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration II-451 Me Et Me NH iPr CH₂ H racemic II-452 Me Et Me NH iPr CH₂ H (S)- II-453 Me Me Me N(Me) iPr CH₂ H racemic II-454 Me Me Me N(Me) iPr CH₂ H (S)- II-455 Me Et Me N(Me) iPr CH₂ H racemic II-456 Me Et Me N(Me) iPr CH₂ H (S)- II-457 Me Me Me NH cHex CH₂ H racemic II-458 Me Me Me NH cHex CH₂ H (S)- II-459 Me Et Me NH cHex CH₂ H racemic II-460 Me Et Me NH cHex CH₂ H (S)- II-461 Me Me Me N(Me) cHex CH₂ H racemic II-462 Me Me Me N(Me) cHex CH₂ H (S)- II-463 Me Et Me N(Me) cHex CH₂ H racemic II-464 Me Et Me N(Me) cHex CH₂ H (S)- II-465 Me Me Me NH 1,3-Benzodi- CH₂ H racemic oxol-4-yl II-466 Me Me Me NH 1,3-Benzodi- CH₂ H (S)- oxol-4-yl II-467 Me Et Me NH 1,3-Benzodi- CH₂ H racemic oxol-4-yl II-468 Me Et Me NH 1,3-Benzodi- CH₂ H (S)- oxol-4-yl II-469 Me Me Me N(Me) 1,3-Benzodi- CH₂ H racemic oxol-4-yl II-470 Me Me Me N(Me) 1,3 -Benzodi- CH₂ H (S)- oxol-4-yl II-471 Me Et Me N(Me) 1,3-Benzodi- CH₂ H racemic oxol-4-yl II-472 Me Et Me N(Me) 1,3-Benzodi- CH₂ H (S)- oxol-4-yl II-473 Me Me Me NH 2-F—Ph CH₂ H racemic II-474 Me Me Me NH 2-F—Ph CH₂ H (S)- II-475 Me Et Me NH 2-F—Ph CH₂ H racemic II-476 Me Et Me NH 2-F—Ph CH₂ H (S)- II-477 Me Me Me N(Me) 2-F—Ph CH₂ H racemic II-478 Me Me Me N(Me) 2-F—Ph CH₂ H (S)- II-479 Me Et Me N(Me) 2-F—Ph CH₂ H racemic II-480 Me Et Me N(Me) 2-F—Ph CH₂ H (S)- II-481 Me Me Me NH 3-F—Ph CH₂ H racemic II-482 Me Me Me NH 3-F—Ph CH₂ H (S)- II-483 Me Et Me NH 3-F—Ph CH₂ H racemic II-484 Me Et Me NH 3-F—Ph CH₂ H (S)- II-485 Me Me Me N(Me) 3-F—Ph CH₂ H racemic II-486 Me Me Me N(Me) 3-F—Ph CH₂ H (S)- II-487 Me Et Me N(Me) 3-F—Ph CH₂ H racemic II-488 Me Et Me N(Me) 3-F—Ph CH₂ H (S)- II-489 Me Me Me NH 4-F—Ph CH₂ H racemic II-490 Me Me Me NH 4-F—Ph CH₂ H (S)- II-491 Me Et Me NH 4-F—Ph CH₂ H racemic II-492 Me Et Me NH 4-F—Ph CH₂ H (S)- II-493 Me Me Me N(Me) 4-F—Ph CH₂ H racemic II-494 Me Me Me N(Me) 4-F—Ph CH₂ H (S)- II-495 Me Et Me N(Me) 4-F—Ph CH₂ H racemic II-496 Me Et Me N(Me) 4-F—Ph CH₂ H (S)- II-497 Me Me Me NH 2-Py CH₂ H racemic II-498 Me Me Me NH 2-Py CH₂ H (S)- II-499 Me Et Me NH 2-Py CH₂ H racemic II-500 Me Et Me NH 2-Py CH₂ H (S)-

TABLE 19 (II)

Compound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration II-501 Me Me Me N(Me) 2-Py CH₂ H racemic II-502 Me Me Me N(Me) 2-Py CH₂ H (S)- II-503 Me Et Me N(Me) 2-Py CH₂ H racemic II-504 Me Et Me N(Me) 2-Py CH₂ H (S)- II-505 Me Me Me NH 3-Py CH₂ H racemic II-506 Me Me Me NH 3-Py CH₂ H (S)- II-507 Me Et Me NH 3-Py CH₂ H racemic II-508 Me Et Me NH 3-Py CH₂ H (S)- II-509 Me Me Me N(Me) 3-Py CH₂ H racemic II-510 Me Me Me N(Me) 3-Py CH₂ H (S)- II-511 Me Et Me N(Me) 3-Py CH₂ H racemic II-512 Me Et Me N(Me) 3-Py CH₂ H (S)- II-513 Me Me Me NH 4-Py CH₂ H racemic II-514 Me Me Me NH 4-Py CH₂ H (S)- II-515 Me Et Me NH 4-Py CH₂ H racemic II-516 Me Et Me NH 4-Py CH₂ H (S)- II-517 Me Me Me N(Me) 4-Py CH₂ H racemic II-518 Me Me Me N(Me) 4-Py CH₂ H (S)- II-519 Me Et Me N(Me) 4-Py CH₂ H racemic II-520 Me Et Me N(Me) 4-Py CH₂ H (S)- II-521 Me Me Me CH₂ Ph CH₂ H racemic II-522 Me Me Me CH₂ Ph CH₂ H (S)- II-523 Me Et Me CH₂ Ph CH₂ H racemic II-524 Me Et Me CH₂ Ph CH₂ H (S)- II-525 Me Me Me CH₂ Ph — H racemic II-526 Me Me Me CH₂ Ph — H (S)- II-527 Me Et Me CH₂ Ph — H racemic II-528 Me Et Me CH₂ Ph — H (S)- II-529 Me Me Me CH₂ Ph CH₂ Me racemic II-530 Me Me Me CH₂ Ph CH₂ Me (S)- II-531 Me Et Me CH₂ Ph CH₂ Me racemic II-532 Me Et Me CH₂ Ph CH₂ Me (S)- II-533 Me Me Me CH₂ Ph C(Me)₂ H racemic II-534 Me Me Me CH₂ Ph C(Me)₂ H (S)- II-535 Me Et Me CH₂ Ph C(Me)₂ H racemic II-536 Me Et Me CH₂ Ph C(Me)₂ H (S)- II-537 Me Me Me CH₂ Ph C(Me)₂ Me racemic II-538 Me Me Me CH₂ Ph C(Me)₂ Me (S)- II-539 Me Et Me CH₂ Ph C(Me)₂ Me racemic II-540 Me Et Me CH₂ Ph C(Me)₂ Me (S)- II-541 Me Me Me CH₂ Ph (CH₂)₂ H racemic II-542 Me Me Me CH₂ Ph (CH₂)₂ H (S)- II-543 Me Et Me CH₂ Ph (CH₂)₂ H racemic II-544 Me Et Me CH₂ Ph (CH₂)₂ H (S)- II-545 Me Me Me CH₂ Ph (CH₂)₂ Me racemic II-546 Me Me Me CH₂ Ph (CH₂)₂ Me (S)- II-547 Me Et Me CH₂ Ph (CH₂)₂ Me racemic II-548 Me Et Me CH₂ Ph (CH₂)₂ Me (S)- II-549 Me Me Me CH₂ Ph CH₂C(Me)₂ H racemic II-550 Me Me Me CH₂ Ph CH₂C(Me)₂ H (S)-

TABLE 20 (II)

Compound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration II-551 Me Et Me CH₂ Ph CH₂C(Me)₂ H racemic II-552 Me Et Me CH₂ Ph CH₂C(Me)₂ H (S)- II-553 Me Me Me CH₂ Ph CH₂C(Me)₂ Me racemic II-554 Me Me Me CH₂ Ph CH₂C(Me)₂ Me (S)- II-555 Me Et Me CH₂ Ph CH₂C(Me)₂ Me racemic II-556 Me Et Me CH₂ Ph CH₂C(Me)₂ Me N- II-557 Me Me Me — Ph CH₂ H racemic II-558 Me Me Me — Ph CH₂ H (S)- II-559 Me Me Me — Ph CH₂ Me racemic II-560 Me Me Me — Ph CH₂ Me (S)- II-561 Me Me Me CH═CH Ph CH₂ H racemic II-562 Me Me Me CH═CH Ph CH₂ H (S)- II-563 Me Me Me CH═CH Ph CH₂ Me racemic II-564 Me Me Me CH═CH Ph CH₂ Me (S)- II-565 Me Me Me C≡C Ph CH₂ H racemic II-566 Me Me Me C≡C Ph CH₂ H (S)- II-567 Me Me Me C≡C Ph CH₂ Me racemic II-568 Me Me Me C≡C Ph CH₂ Me (S)- II-569 Me Me Me 1,2-Cyclopro- Ph CH₂ H racemic pylene II-570 Me Me Me 1,2-Cyclopro- Ph CH₂ H (S)- pylene II-571 Me Me Me 1,2-Cyclopro- Ph CH₂ Me racemic pylene II-572 Me Me Me 1,2-Cyclopro- Ph CH₂ Me (S)- pylene II-573 Me Me Me 1,2-Cyclopro- Ph CH₂ H racemic pynylene II-574 Me Me Me 1,2-Cyclopro- Ph CH₂ H (S)- pynylene II-575 Me Me Me 1,2-Cyclopro- Ph CH₂ Me racemic pynylene II-576 Me Me Me 1,2-Cyclopro- Ph CH₂ Me (S)- pynylene

TABLE 21 (II)

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration II-577 Me Me Me O Ph C(Me)₂CH₂ H racemic II-578 Me Me Me O Ph C(Me)₂CH₂ H (+) II-579 Me Me Me O Ph C(Me)₂CH₂ H (−) II-580 Me Et Me O Ph C(Me)₂CH₂ H racemic II-581 Me Et Me O Ph C(Me)₂CH₂ H (+) II-582 Me Et Me O Ph C(Me)₂CH₂ H (−) II-583 Me Me Me O Ph C(Me)₂CH₂ Me racemic II-584 Me Me Me O Ph C(Me)₂CH₂ Me (+) II-585 Me Me Me O Ph C(Me)₂CH₂ Me (−) II-586 Me Et Me O Ph C(Me)₂CH₂ Me racemic II-587 Me Et Me O Ph C(Me)₂CH₂ Me (+) II-588 Me Et Me O Ph C(Me)₂CH₂ Me (−) II-589 Me Me Me O Ph C(Me)₂CH₂ CHF₂ racemic II-590 Me Me Me O Ph C(Me)₂CH₂ CHF₂ (+) II-591 Me Me Me O Ph C(Me)₂CH₂ CHF₂ (−) II-592 Me Me Me O Ph C(Me)₂CH₂ Et racemic II-593 Me Me Me O Ph C(Me)₂CH₂ Et (+) II-594 Me Me Me O Ph C(Me)₂CH₂ Et (−) II-595 Me Me Me NH Ph C(Me)₂CH₂ H (+) II-596 Me Me Me NH Ph C(Me)₂CH₂ H (−) II-597 Me Et Me NH Ph C(Me)₂CH₂ H (+) II-598 Me Et Me NH Ph C(Me)₂CH₂ H (−) II-599 Me Me Me NH Ph C(Me)₂CH₂ Me racemic II-600 Me Me Me NH Ph C(Me)₂CH₂ Me (+) II-601 Me Me Me NH Ph C(Me)₂CH₂ Me (−) II-602 Me Et Me NH Ph C(Me)₂CH₂ Me racemic II-603 Me Et Me NH Ph C(Me)₂CH₂ Me (+) II-604 Me Et Me NH Ph C(Me)₂CH₂ Me (−) II-605 Me Me Me NH Ph C(Me)₂CH₂ CHF₂ racemic II-606 Me Me Me NH Ph C(Me)₂CH₂ CHF₂ (+) II-607 Me Me Me NH Ph C(Me)₂CH₂ CHF₂ (−) II-608 Me Et Me NH Ph C(Me)₂CH₂ CHF₂ racemic II-609 Me Et Me NH Ph C(Me)₂CH₂ CHF₂ (+) II-610 Me Et Me NH Ph C(Me)₂CH₂ CHF₂ (−) II-611 Me Me Me NH Ph C(Me)₂CH₂ Et racemic II-612 Me Me Me NH Ph C(Me)₂CH₂ Et (+) II-613 Me Me Me NH Ph C(Me)₂CH₂ Et (−) II-614 Me Et Me NH Ph C(Me)₂CH₂ Et racemic II-615 Me Et Me NH Ph C(Me)₂CH₂ Et (+) II-616 Me Et Me NH Ph C(Me)₂CH₂ Et (−) II-617 Me Me Me NH Ph C(Me)₂CH₂ iPr racemic II-618 Me Me Me NH Ph C(Me)₂CH₂ iPr (+) II-619 Me Me Me NH Ph C(Me)₂CH₂ iPr (−) II-620 Me Et Me NH Ph C(Me)₂CH₂ iPr racemic II-621 Me Et Me NH Ph C(Me)₂CH₂ iPr (+) II-622 Me Et Me NH Ph C(Me)₂CH₂ iPr (−) II-623 Me Me Me NH Ph C(Me)₂CH₂ cPr racemic II-624 Me Me Me NH Ph C(Me)₂CH₂ cPr (+) II-625 Me Me Me NH Ph C(Me)₂CH₂ cPr (−) II-626 Me Et Me NH Ph C(Me)₂CH₂ cPr racemic

TABLE 22 (II)

Com- pound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration II-627 Me Et Me NH Ph C(Me)₂CH₂ cPr (+) II-628 Me Et Me NH Ph C(Me)₂CH₂ cPr (−) II-629 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ H racemic II-630 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ H (+) II-631 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ H (−) II-632 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ H racemic II-633 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ H (+) II-634 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ H (−) II-635 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ Me racemic II-636 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ Me (+) II-637 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ Me (−) II-638 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ Me racemic II-639 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ Me (+) II-640 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ Me (−) II-641 Me Me Me NH Ph 1,1-Cyclobutylene-CH₂ H racemic II-642 Me Me Me NH Ph 1,1-Cyclobutylene-CH₂ H (+) II-643 Me Me Me NH Ph 1,1-Cyclobutylene-CH₂ H (−) II-644 Me Et Me NH Ph 1,1-Cyclobutylene-CH₂ H racemic II-645 Me Et Me NH Ph 1,1-Cyclobutylene-CH₂ H (+) II-646 Me Et Me NH Ph 1,1-Cyclobutylene-CH₂ H (−) II-647 Me Me Me NH Ph 1,1-Cyclobutylene-CH₂ Me racemic II-648 Me Me Me NH Ph 1,1-Cyclobutylene-CH₂ Me (+) II-649 Me Me Me NH Ph 1,1-Cyclobutylene-CH₂ Me (−) II-650 Me Et Me NH Ph 1,1-Cyclobutylene-CH₂ Me racemic II-651 Me Et Me NH Ph 1,1-Cyclobutylene-CH₂ Me (+) II-652 Me Et Me NH Ph 1,1-Cyclobutylene-CH₂ Me (−) II-653 Me Me Me NH Ph C(Et)₂CH₂ H racemic II-654 Me Me Me NH Ph C(Et)₂CH₂ H (+) II-655 Me Me Me NH Ph C(Et)₂CH₂ H (−) II-656 Me Et Me NH Ph C(Et)₂CH₂ H racemic II-657 Me Et Me NH Ph C(Et)₂CH₂ H (+) II-658 Me Et Me NH Ph C(Et)₂CH₂ H (−) II-659 Me Me Me NH Ph C(Et)₂CH₂ Me racemic II-660 Me Me Me NH Ph C(Et)₂CH₂ Me (+) II-661 Me Me Me NH Ph C(Et)₂CH₂ Me (−) II-662 Me Et Me NH Ph C(Et)₂CH₂ Me racemic II-663 Me Et Me NH Ph C(Et)₂CH₂ Me (+) II-664 Me Et Me NH Ph C(Et)₂CH₂ Me (−) II-665 Me Me Me NH Ph CH₂-1,1-Cyclopropylene H racemic II-666 Me Me Me NH Ph CH₂-1,1-Cyclopropylene H (R)- II-667 Me Et Me NH Ph CH₂-1,1-Cyclopropylene H racemic II-668 Me Et Me NH Ph CH₂-1,1-Cyclopropylene H (R)- II-669 Me Me Me NH Ph CH₂-1,1-Cyclopropylene Me racemic II-670 Me Me Me NH Ph CH₂-1,1-Cyclopropylene Me (R)- II-671 Me Et Me NH Ph CH₂-1,1-Cyclopropylene Me racemic II-672 Me Et Me NH Ph CH₂-1,1-Cyclopropylene Me (R)- II-673 Me Me Me NH Ph CH₂-1,1-cyclobutylene H racemic II-674 Me Me Me NH Ph CH₂-1,1-cyclobutylene H (R)- II-675 Me Et Me NH Ph CH₂-1,1-cyclobutylene H racemic II-676 Me Et Me NH Ph CH₂-1,1-cyclobutylene H (R)-

TABLE 23 (II)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration II-677 Me Me Me NH Ph CH₂-1,1- Me racemic cyclobutylene II-678 Me Me Me NH Ph CH₂-1,1- Me (R)- cyclobutylene II-679 Me Et Me NH Ph CH₂-1,1- Me racemic cyclobutylene II-680 Me Et Me NH Ph CH₂-1,1- Me (R)- cyclobutylene II-681 Me Me Me NH Ph CH₂C(Et)₂ H racemic II-682 Me Me Me NH Ph CH₂C(Et)₂ H (R)- II-683 Me Et Me NH Ph CH₂C(Et)₂ H racemic II-684 Me Et Me NH Ph CH₂C(Et)₂ H (R)- II-685 Me Me Me NH Ph CH₂C(Et)₂ Me racemic II-686 Me Me Me NH Ph CH₂C(Et)₂ Me (R)- II-687 Me Et Me NH Ph CH₂C(Et)₂ Me racemic II-688 Me Et Me NH Ph CH₂C(Et)₂ Me (R)- II-689 Me Me Me NH iPr CH₂ Me racemic II-690 Me Me Me NH iPr CH₂ Me (S)- II-691 Me Et Me NH iPr CH₂ Me racemic II-692 Me Et Me NH iPr CH₂ Me (S)- II-693 Me Me Me NH iPr (CH₂)₂ H racemic II-694 Me Me Me NH iPr (CH₂)₂ H (R)- II-695 Me Et Me NH iPr (CH₂)₂ H racemic II-696 Me Et Me NH iPr (CH₂)₂ H (R)- II-697 Me Me Me NH iPr (CH₂)₂ Me racemic II-698 Me Me Me NH iPr (CH₂)₂ Me (R)- II-699 Me Et Me NH iPr (CH₂)₂ Me racemic II-700 Me Et Me NH iPr (CH₂)₂ Me (R)- II-701 Me Me Me NH CF₃ CH₂ H racemic II-702 Me Me Me NH CF₃ CH₂ H (S)- II-703 Me Et Me NH CF₃ CH₂ H racemic II-704 Me Et Me NH CF₃ CH₂ H (S)- II-705 Me Me Me NH CH₂OH CH₂ H II-706 Me Et Me NH CH₂OH CH₂ H II-707 Me Me Me NH CH₂OMe CH₂ H racemic II-708 Me Me Me NH CH₂OMe CH₂ H (R)- II-709 Me Et Me NH CH₂OMe CH₂ H racemic II-710 Me Et Me NH CH₂OMe CH₂ H (R)- II-711 Me Me Me NH CH₂Ph CH₂ H racemic II-712 Me Me Me NH CH₂Ph CH₂ H (R)- II-713 Me Me Me NH CH₂Ph CH₂ H (S)- II-714 Me Et Me NH CH₂Ph CH₂ H racemic II-715 Me Et Me NH CH₂Ph CH₂ H (S)- II-716 Me Me Me NH 2-F—Ph CH₂ Me racemic II-717 Me Me Me NH 2-F—Ph CH₂ Me (S)- II-718 Me Et Me NH 2-F—Ph CH₂ Me racemic II-719 Me Et Me NH 2-F—Ph CH₂ Me (S)- II-720 Me Me Me NH 2-F—Ph (CH₂)₂ H racemic II-721 Me Me Me NH 2-F—Ph (CH₂)₂ H (R)- II-722 Me Et Me NH 2-F—Ph (CH₂)₂ H racemic II-723 Me Et Me NH 2-F—Ph (CH₂)₂ H (R)- II-724 Me Me Me NH 2-F—Ph (CH₂)₂ Me racemic II-725 Me Me Me NH 2-F—Ph (CH₂)₂ Me (R)- II-726 Me Et Me NH 2-F—Ph (CH₂)₂ Me racemic

TABLE 24 (II)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration II-727 Me Et Me NH 2-F—Ph (CH₂)₂ Me (R)- II-728 Me Me Me NH 2-F—Ph CH₂C(Me)₂ H racemic II-729 Me Me Me NH 2-F—Ph CH₂C(Me)₂ H (R)- II-730 Me Et Me NH 2-F—Ph CH₂C(Me)₂ H racemic II-731 Me Et Me NH 2-F—Ph CH₂C(Me)₂ H (R)- II-732 Me Me Me NH 2-F—Ph CH₂C(Me)₂ Me racemic II-733 Me Me Me NH 2-F—Ph CH₂C(Me)₂ Me (R)- II-734 Me Et Me NH 2-F—Ph CH₂C(Me)₂ Me racemic II-735 Me Et Me NH 2-F—Ph CH₂C(Me)₂ Me (R)- II-736 Me Me Me NH 2-F—Ph C(Me)₂CH₂ H racemic II-737 Me Me Me NH 2-F—Ph C(Me)₂CH₂ H (+) II-738 Me Me Me NH 2-F—Ph C(Me)₂CH₂ H (−) II-739 Me Et Me NH 2-F—Ph C(Me)₂CH₂ H racemic II-740 Me Et Me NH 2-F—Ph C(Me)₂CH₂ H (+) II-741 Me Et Me NH 2-F—Ph C(Me)₂CH₂ H (−) II-742 Me Me Me NH 2-F—Ph C(Me)₂CH₂ Me racemic II-743 Me Me Me NH 2-F—Ph C(Me)₂CH₂ Me (+) II-744 Me Me Me NH 2-F—Ph C(Me)₂CH₂ Me (−) II-745 Me Et Me NH 2-F—Ph C(Me)₂CH₂ Me racemic II-746 Me Et Me NH 2-F—Ph C(Me)₂CH₂ Me (+) II-747 Me Et Me NH 2-F—Ph C(Me)₂CH₂ Me (−) II-748 Me Me Me NH 3-F—Ph (CH₂)₂ H racemic II-749 Me Me Me NH 3-F—Ph (CH₂)₂ H (R)- II-750 Me Et Me NH 3-F—Ph (CH₂)₂ H racemic II-751 Me Et Me NH 3-F—Ph (CH₂)₂ H (R)- II-752 Me Me Me NH 3-F—Ph (CH₂)₂ Me racemic II-753 Me Me Me NH 3-F—Ph (CH₂)₂ Me (R)- II-754 Me Et Me NH 3-F—Ph (CH₂)₂ Me racemic II-755 Me Et Me NH 3-F—Ph (CH₂)₂ Me (R)- II-756 Me Me Me NH 3-F—Ph CH₂C(Me)₂ H racemic II-757 Me Me Me NH 3-F—Ph CH₂C(Me)₂ H (R)- II-758 Me Et Me NH 3-F—Ph CH₂C(Me)₂ H racemic II-759 Me Et Me NH 3-F—Ph CH₂C(Me)₂ H (R)- II-760 Me Me Me NH 3-F—Ph CH₂C(Me)₂ Me racemic II-761 Me Me Me NH 3-F—Ph CH₂C(Me)₂ Me (R)- II-762 Me Et Me NH 3-F—Ph CH₂C(Me)₂ Me racemic II-763 Me Et Me NH 3-F—Ph CH₂C(Me)₂ Me (R)- II-764 Me Me Me NH 3-F—Ph C(Me)₂CH₂ H racemic II-765 Me Me Me NH 3-F—Ph C(Me)₂CH₂ H (+) II-766 Me Me Me NH 3-F—Ph C(Me)₂CH₂ H (−) II-767 Me Et Me NH 3-F—Ph C(Me)₂CH₂ H racemic II-768 Me Et Me NH 3-F—Ph C(Me)₂CH₂ H (+) II-769 Me Et Me NH 3-F—Ph C(Me)₂CH₂ H (−) II-770 Me Me Me NH 3-F—Ph C(Me)₂CH₂ Me racemic II-771 Me Me Me NH 3-F—Ph C(Me)₂CH₂ Me (+) II-772 Me Me Me NH 3-F—Ph C(Me)₂CH₂ Me (−) II-773 Me Et Me NH 3-F—Ph C(Me)₂CH₂ Me racemic II-774 Me Et Me NH 3-F—Ph C(Me)₂CH₂ Me (+) II-775 Me Et Me NH 3-F—Ph C(Me)₂CH₂ Me (−) II-776 Me Me Me NH 4-F—Ph (CH₂)₂ H racemic

TABLE 25 (II)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration II-777 Me Me Me NH 4-F—Ph (CH₂)₂ H (R)- II-778 Me Et Me NH 4-F—Ph (CH₂)₂ H racemic II-779 Me Et Me NH 4-F—Ph (CH₂)₂ H (R)- II-780 Me Me Me NH 4-F—Ph (CH₂)₂ Me racemic II-781 Me Me Me NH 4-F—Ph (CH₂)₂ Me (R)- II-782 Me Et Me NH 4-F—Ph (CH₂)₂ Me racemic II-783 Me Et Me NH 4-F—Ph (CH₂)₂ Me (R)- II-784 Me Me Me NH 4-F—Ph CH₂C(Me)₂ H racemic II-785 Me Me Me NH 4-F—Ph CH₂C(Me)₂ H (R)- II-786 Me Et Me NH 4-F—Ph CH₂C(Me)₂ H racemic II-787 Me Et Me NH 4-F—Ph CH₂C(Me)₂ H (R)- II-788 Me Me Me NH 4-F—Ph CH₂C(Me)₂ Me racemic II-789 Me Me Me NH 4-F—Ph CH₂C(Me)₂ Me (R)- II-790 Me Et Me NH 4-F—Ph CH₂C(Me)₂ Me racemic II-791 Me Et Me NH 4-F—Ph CH₂C(Me)₂ Me (R)- II-792 Me Me Me NH 4-F—Ph C(Me)₂CH₂ H racemic II-793 Me Me Me NH 4-F—Ph C(Me)₂CH₂ H (+) II-794 Me Me Me NH 4-F—Ph C(Me)₂CH₂ H (−) II-795 Me Et Me NH 4-F—Ph C(Me)₂CH₂ H racemic II-796 Me Et Me NH 4-F—Ph C(Me)₂CH₂ H (+) II-797 Me Et Me NH 4-F—Ph C(Me)₂CH₂ H (−) II-798 Me Me Me NH 4-F—Ph C(Me)₂CH₂ Me racemic II-799 Me Me Me NH 4-F—Ph C(Me)₂CH₂ Me (+) II-800 Me Me Me NH 4-F—Ph C(Me)₂CH₂ Me (−) II-801 Me Et Me NH 4-F—Ph C(Me)₂CH₂ Me racemic II-802 Me Et Me NH 4-F—Ph C(Me)₂CH₂ Me (+) II-803 Me Et Me NH 4-F—Ph C(Me)₂CH₂ Me (−) II-804 Me Me Me NH 2-Cl—Ph CH₂ H racemic II-805 Me Me Me NH 2-Cl—Ph CH₂ H (S)- II-806 Me Et Me NH 2-Cl—Ph CH₂ H racemic II-807 Me Et Me NH 2-Cl—Ph CH₂ H (S)- II-808 Me Me Me NH 2-Cl—Ph CH₂ Me racemic II-809 Me Me Me NH 2-Cl—Ph CH₂ Me (S)- II-810 Me Et Me NH 2-Cl—Ph CH₂ Me racemic II-811 Me Et Me NH 2-Cl—Ph CH₂ Me (S)- II-812 Me Me Me NH 2-Cl—Ph (CH₂)₂ H racemic II-813 Me Me Me NH 2-Cl—Ph (CH₂)₂ H (R)- II-814 Me Et Me NH 2-Cl—Ph (CH₂)₂ H racemic II-815 Me Et Me NH 2-Cl—Ph (CH₂)₂ H (R)- II-816 Me Me Me NH 2-Cl—Ph (CH₂)₂ Me racemic II-817 Me Me Me NH 2-Cl—Ph (CH₂)₂ Me (R)- II-818 Me Et Me NH 2-Cl—Ph (CH₂)₂ Me racemic II-819 Me Et Me NH 2-Cl—Ph (CH₂)₂ Me (R)- II-820 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ H racemic II-821 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ H (R)- II-822 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ H racemic II-823 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ H (R)- II-824 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ Me racemic II-825 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ Me (R)- II-826 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ Me racemic

TABLE 26 (II)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration II-827 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ Me (R)- II-828 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ H racemic II-829 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ H (+) II-830 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ H (−) II-831 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ H racemic II-832 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ H (+) II-833 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ H (−) II-834 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ Me racemic II-835 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ Me (+) II-836 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ Me (−) II-837 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ Me racemic II-838 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ Me (+) II-839 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ Me (−) II-840 Me Me Me NH 3-Cl—Ph CH₂ H racemic II-841 Me Me Me NH 3-Cl—Ph CH₂ H (S)- II-842 Me Et Me NH 3-Cl—Ph CH₂ H racemic II-843 Me Et Me NH 3-Cl—Ph CH₂ H (S)- II-844 Me Me Me NH 3-Cl—Ph CH₂ Me racemic II-845 Me Me Me NH 3-Cl—Ph CH₂ Me (S)- II-846 Me Et Me NH 3-Cl—Ph CH₂ Me racemic II-847 Me Et Me NH 3-Cl—Ph CH₂ Me (S)- II-848 Me Me Me NH 3-Cl—Ph (CH₂)₂ H racemic II-849 Me Me Me NH 3-Cl—Ph (CH₂)₂ H (R)- II-850 Me Et Me NH 3-Cl—Ph (CH₂)₂ H racemic II-851 Me Et Me NH 3-Cl—Ph (CH₂)₂ H (R)- II-852 Me Me Me NH 3-Cl—Ph (CH₂)₂ Me racemic II-853 Me Me Me NH 3-Cl—Ph (CH₂)₂ Me (R)- II-854 Me Et Me NH 3-Cl—Ph (CH₂)₂ Me racemic II-855 Me Et Me NH 3-Cl—Ph (CH₂)₂ Me (R)- II-856 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ H racemic II-857 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ H (R)- II-858 Me Et Me NH 3-Cl—Ph CH₂C(Me)₂ H racemic II-859 Me Et Me NH 3-Cl—Ph CH₂C(Me)₂ H (R)- II-860 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ Me racemic II-861 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ Me (R)- II-862 Me Et Me NH 3-Cl—Ph CH₂C(Me)₂ Me racemic II-863 Me Et Me NH 3-Cl—Ph CH₂C(Me)₂ Me (R)- II-864 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ H racemic II-865 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ H (+) II-866 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ H (−) II-867 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ H racemic II-868 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ H (+) II-869 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ H (−) II-870 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ Me racemic II-871 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ Me (+) II-872 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ Me (−) II-873 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ Me racemic II-874 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ Me (+) II-875 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ Me (−) II-876 Me Me Me NH 4-Cl—Ph CH₂ H racemic

TABLE 27 (II)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration II-877 Me Me Me NH 4-Cl—Ph CH₂ H (S)- II-878 Me Et Me NH 4-Cl—Ph CH₂ H racemic II-879 Me Et Me NH 4-Cl—Ph CH₂ H (S)- II-880 Me Me Me NH 4-Cl—Ph CH₂ Me racemic II-881 Me Me Me NH 4-Cl—Ph CH₂ Me (S)- II-882 Me Et Me NH 4-Cl—Ph CH₂ Me racemic II-883 Me Et Me NH 4-Cl—Ph CH₂ Me (S)- II-884 Me Me Me NH 4-Cl—Ph (CH₂)₂ H racemic II-885 Me Me Me NH 4-Cl—Ph (CH₂)₂ H (R)- II-886 Me Et Me NH 4-Cl—Ph (CH₂)₂ H racemic II-887 Me Et Me NH 4-Cl—Ph (CH₂)₂ H (R)- II-888 Me Me Me NH 4-Cl—Ph (CH₂)₂ Me racemic II-889 Me Me Me NH 4-Cl—Ph (CH₂)₂ Me (R)- II-890 Me Et Me NH 4-Cl—Ph (CH₂)₂ Me racemic II-891 Me Et Me NH 4-Cl—Ph (CH₂)₂ Me (R)- II-892 Me Me Me NH 4-Cl—Ph CH₂C(Me)₂ H racemic II-893 Me Me Me NH 4-Cl—Ph CH₂C(Me)₂ H (R)- II-894 Me Et Me NH 4-Cl—Ph CH₂C(Me)₂ H racemic II-895 Me Et Me NH 4-Cl—Ph CH₂C(Me)₂ H (R)- II-896 Me Me Me NH 4-Cl—Ph CH₂C(Me)₂ Me racemic II-897 Me Me Me NH 4-Cl—Ph CH₂C(Me)₂ Me (R)- II-898 Me Et Me NH 4-Cl—Ph CH₂C(Me)₂ Me racemic II-899 Me Et Me NH 4-Cl—Ph CH₂C(Me)₂ Me (R)- II-900 Me Me Me NH 4-Cl—Ph C(Me)₂CH₂ H racemic II-901 Me Me Me NH 4-Cl—Ph C(Me)₂CH₂ H (+) II-902 Me Me Me NH 4-Cl—Ph C(Me)₂CH₂ H (−) II-903 Me Et Me NH 4-Cl—Ph C(Me)₂CH₂ H racemic II-904 Me Et Me NH 4-Cl—Ph C(Me)₂CH₂ H (+) II-905 Me Et Me NH 4-Cl—Ph C(Me)₂CH₂ H (−) II-906 Me Me Me NH 4-Cl—Ph C(Me)₂CH₂ Me racemic II-907 Me Me Me NH 4-Cl—Ph C(Me)₂CH₂ Me (+) II-908 Me Me Me NH 4-Cl—Ph C(Me)₂CH₂ Me (−) II-909 Me Et Me NH 4-Cl—Ph C(Me)₂CH₂ Me racemic II-910 Me Et Me NH 4-Cl—Ph C(Me)₂CH₂ Me (+) II-911 Me Et Me NH 4-Cl—Ph C(Me)₂CH₂ Me (−) II-912 Me Me Me NH 2-Me—Ph CH₂ H racemic II-913 Me Me Me NH 2-Me—Ph CH₂ H (S)- II-914 Me Et Me NH 2-Me—Ph CH₂ H racemic II-915 Me Et Me NH 2-Me—Ph CH₂ H (S)- II-916 Me Me Me NH 2-Me—Ph CH₂ Me racemic II-917 Me Me Me NH 2-Me—Ph CH₂ Me (S)- II-918 Me Et Me NH 2-Me—Ph CH₂ Me racemic II-919 Me Et Me NH 2-Me—Ph CH₂ Me (S)- II-920 Me Me Me NH 2-Me—Ph (CH₂)₂ H racemic II-921 Me Me Me NH 2-Me—Ph (CH₂)₂ H (R)- II-922 Me Et Me NH 2-Me—Ph (CH₂)₂ H racemic II-923 Me Et Me NH 2-Me—Ph (CH₂)₂ H (R)- II-924 Me Me Me NH 2-Me—Ph (CH₂)₂ Me racemic II-925 Me Me Me NH 2-Me—Ph (CH₂)₂ Me (R)- II-926 Me Et Me NH 2-Me—Ph (CH₂)₂ Me racemic

TABLE 28 (II)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration II-927 Me Et Me NH 2-Me—Ph (CH₂)₂ Me (R)- II-928 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ H racemic II-929 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ H (R)- II-930 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ H racemic II-931 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ H (R)- II-932 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ Me racemic II-933 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ Me (R)- II-934 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ Me racemic II-935 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ Me (R)- II-936 Me Me Me NH 2-Me—Ph C(Me)₂CH₂ H racemic II-937 Me Me Me NH 2-Me—Ph C(Me)₂CH₂ H (+) II-938 Me Me Me NH 2-Me—Ph C(Me)₂CH₂ H (−) II-939 Me Et Me NH 2-Me—Ph C(Me)₂CH₂ H racemic II-940 Me Et Me NH 2-Me—Ph C(Me)₂CH₂ H (+) II-941 Me Et Me NH 2-Me—Ph C(Me)₂CH₂ H (−) II-942 Me Me Me NH 2-Me—Ph C(Me)₂CH₂ Me racemic II-943 Me Me Me NH 2-Me—Ph C(Me)₂CH₂ Me (+) II-944 Me Me Me NH 2-Me—Ph C(Me)₂CH₂ Me (−) II-945 Me Et Me NH 2-Me—Ph C(Me)₂CH₂ Me racemic II-946 Me Et Me NH 2-Me—Ph C(Me)₂CH₂ Me (+) II-947 Me Et Me NH 2-Me—Ph C(Me)₂CH₂ Me (−) II-948 Me Me Me NH 3-Me—Ph CH₂ H racemic II-949 Me Me Me NH 3-Me—Ph CH₂ H (S)- II-950 Me Et Me NH 3-Me—Ph CH₂ H racemic II-951 Me Et Me NH 3-Me—Ph CH₂ H (S)- II-952 Me Me Me NH 3-Me—Ph CH₂ Me racemic II-953 Me Me Me NH 3-Me—Ph CH₂ Me (S)- II-954 Me Et Me NH 3-Me—Ph CH₂ Me racemic II-955 Me Et Me NH 3-Me—Ph CH₂ Me (S)- II-956 Me Me Me NH 3-Me—Ph (CH₂)₂ H racemic II-957 Me Me Me NH 3-Me—Ph (CH₂)₂ H (R)- II-958 Me Et Me NH 3-Me—Ph (CH₂)₂ H racemic II-959 Me Et Me NH 3-Me—Ph (CH₂)₂ H (R)- II-960 Me Me Me NH 3-Me—Ph (CH₂)₂ Me racemic II-961 Me Me Me NH 3-Me—Ph (CH₂)₂ Me (R)- II-962 Me Et Me NH 3-Me—Ph (CH₂)₂ Me racemic II-963 Me Et Me NH 3-Me—Ph (CH₂)₂ Me (R)- II-964 Me Me Me NH 3-Me—Ph CH₂C(Me)₂ H racemic II-965 Me Me Me NH 3-Me—Ph CH₂C(Me)₂ H (R)- II-966 Me Et Me NH 3-Me—Ph CH₂C(Me)₂ H racemic II-967 Me Et Me NH 3-Me—Ph CH₂C(Me)₂ H (R)- II-968 Me Me Me NH 3-Me—Ph CH₂C(Me)₂ Me racemic II-969 Me Me Me NH 3-Me—Ph CH₂C(Me)₂ Me (R)- II-970 Me Et Me NH 3-Me—Ph CH₂C(Me)₂ Me racemic II-971 Me Et Me NH 3-Me—Ph CH₂C(Me)₂ Me (R)- II-972 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ H racemic II-973 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ H (+) II-974 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ H (−) II-975 Me Et Me NH 3-Me—Ph C(Me)₂CH₂ H racemic II-976 Me Et Me NH 3-Me—Ph C(Me)₂CH₂ H (+)

TABLE 29 (II)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration II-977  Me Et Me NH 3-Me—Ph C(Me)₂CH₂ H (−) II-978  Me Me Me NH 3-Me—Ph C(Me)₂CH₂ Me racemic II-979  Me Me Me NH 3-Me—Ph C(Me)₂CH₂ Me (+) II-980  Me Me Me NH 3-Me—Ph C(Me)₂CH₂ Me (−) II-981  Me Et Me NH 3-Me—Ph C(Me)₂CH₂ Me racemic II-982  Me Et Me NH 3-Me—Ph C(Me)₂CH₂ Me (+) II-983  Me Et Me NH 3-Me—Ph C(Me)₂CH₂ Me (−) II-984  Me Me Me NH 4-Me—Ph CH₂ H racemic II-985  Me Me Me NH 4-Me—Ph CH₂ H (S)- II-986  Me Et Me NH 4-Me—Ph CH₂ H racemic II-987  Me Et Me NH 4-Me—Ph CH₂ H (S)- II-988  Me Me Me NH 4-Me—Ph CH₂ Me racemic II-989  Me Me Me NH 4-Me—Ph CH₂ Me (S)- II-990  Me Et Me NH 4-Me—Ph CH₂ Me racemic II-991  Me Et Me NH 4-Me—Ph CH₂ Me (S)- II-992  Me Me Me NH 4-Me—Ph (CH₂)₂ H racemic II-993  Me Me Me NH 4-Me—Ph (CH₂)₂ H (R)- II-994  Me Et Me NH 4-Me—Ph (CH₂)₂ H racemic II-995  Me Et Me NH 4-Me—Ph (CH₂)₂ H (R)- II-996  Me Me Me NH 4-Me—Ph (CH₂)₂ Me racemic II-997  Me Me Me NH 4-Me—Ph (CH₂)₂ Me (R)- II-998  Me Et Me NH 4-Me—Ph (CH₂)₂ Me racemic II-999  Me Et Me NH 4-Me—Ph (CH₂)₂ Me (R)- II-1000 Me Me Me NH 4-Me—Ph CH₂C(Me)₂ H racemic II-1001 Me Me Me NH 4-Me—Ph CH₂C(Me)₂ H (R)- II-1002 Me Et Me NH 4-Me—Ph CH₂C(Me)₂ H racemic II-1003 Me Et Me NH 4-Me—Ph CH₂C(Me)₂ H (R)- II-1004 Me Me Me NH 4-Me—Ph CH₂C(Me)₂ Me racemic II-1005 Me Me Me NH 4-Me—Ph CH₂C(Me)₂ Me (R)- II-1006 Me Et Me NH 4-Me—Ph CH₂C(Me)₂ Me racemic II-1007 Me Et Me NH 4-Me—Ph CH₂C(Me)₂ Me (R)- II-1008 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ H racemic II-1009 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ H (+) II-1010 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ H (−) II-1011 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ H racemic II-1012 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ H (+) II-1013 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ H (−) II-1014 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ Me racemic II-1015 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ Me (+) II-1016 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ Me (−) II-1017 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ Me racemic II-1018 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ Me (+) II-1019 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ Me (−) II-1020 Me Me Me — Ph — H racemic II-1021 Me Me Me — Ph — H (R)- II-1022 Me Et Me — Ph — H racemic II-1023 Me Et Me — Ph — H (R)- II-1024 Me Me Me — Ph — Me racemic II-1025 Me Me Me — Ph — Me (R)- II-1026 Me Et Me — Ph — Me racemic

TABLE 30 (II)

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration II-1027 Me Et Me — Ph — Me (R)- II-1028 Me Me Me — Ph — CHF₂ racemic II-1029 Me Me Me — Ph — CHF₂ (R)- II-1030 Me Et Me — Ph — CHF₂ racemic II-1031 Me Et Me — Ph — CHF₂ (R)- II-1032 Me Me Me — Ph — CF₃ racemic II-1033 Me Me Me — Ph — CF₃ (R)- II-1034 Me Et Me — Ph — CF₃ racemic II-1035 Me Et Me — Ph — CF₃ (R)- II-1036 Me Me Me — Ph — Et racemic II-1037 Me Me Me — Ph — Et (R)- II-1038 Me Et Me — Ph — Et racemic II-1039 Me Et Me — Ph — Et (R)- II-1040 Me Me Me — Ph — CF₂CH₃ racemic II-1041 Me Me Me — Ph — CF₂CH₃ (R)- II-1042 Me Et Me — Ph — CF₂CH₃ racemic II-1043 Me Et Me — Ph — CF₂CH₃ (R)- II-1044 Me Me Me — Ph — nPr racemic II-1045 Me Me Me — Ph — nPr (R)- II-1046 Me Et Me — Ph — nPr racemic II-1047 Me Et Me — Ph — nPr (R)- II-1048 Me Me Me — Ph — nBu racemic II-1049 Me Me Me — Ph — nBu (R)- II-1050 Me Et Me — Ph — nBu racemic II-1051 Me Et Me — Ph — nBu (R)- II-1052 Me Me Me — Ph — iPr racemic II-1053 Me Me Me — Ph — iPr (R)- II-1054 Me Et Me — Ph — iPr racemic II-1055 Me Et Me — Ph — iPr (R)- II-1056 Me Me Me — Ph — cPr racemic II-1057 Me Me Me — Ph — cPr (R)- II-1058 Me Et Me — Ph — cPr racemic II-1059 Me Et Me — Ph — cPr (R)- II-1060 Me Me Me — Ph — Ph racemic II-1061 Me Me Me — Ph — Ph (R)- II-1062 Me Et Me — Ph — Ph racemic II-1063 Me Et Me — Ph — Ph (R)- II-1064 Me Me Me — Ph CH₂ CHF₂ racemic II-1065 Me Me Me — Ph CH₂ CHF₂ (S)- II-1066 Me Me Me — Ph CH₂ Et racemic II-1067 Me Me Me — Ph CH₂ Et (S)- II-1068 Me Me Me — Ph CH₂ Ph racemic II-1069 Me Me Me — Ph CH₂ Ph (R)- II-1070 Me Me Me — Ph (CH₂)₂ H racemic II-1071 Me Me Me — Ph (CH₂)₂ H (S)- II-1072 Me Me Me — Ph (CH₂)₂ Me racemic II-1073 Me Me Me — Ph (CH₂)₂ Me (S)- II-1074 Me Me Me — Ph (CH₂)₂ CHF₂ racemic II-1075 Me Me Me — Ph (CH₂)₂ CHF₂ (S)- II-1076 Me Me Me — Ph (CH₂)₂ Et racemic

TABLE 31 (II)

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration II-1077 Me Me Me — Ph (CH₂)₂ Et (S)- II-1078 Me Me Me — H — H II-1079 Me Me Me — H — Me II-1080 Me Me Me — H — CHF₂ II-1081 Me Me Me — H — CF₃ II-1082 Me Me Me — H — Et II-1083 Me Me Me — H — nPr II-1084 Me Me Me — H — iPr II-1085 Me Me Me — H — cPr II-1086 Me Me Me — H — Ph II-1087 Me Me Me — Me — H racemic II-1088 Me Me Me — Me — H (R)- II-1089 Me Me Me — Me — Me racemic II-1090 Me Me Me — Me — Me (R)- II-1091 Me Me Me — Me — CHF₂ racemic II-1092 Me Me Me — Me — CHF₂ (R)- II-1093 Me Me Me — Me — CF₃ racemic II-1094 Me Me Me — Me — CF₃ (R)- II-1095 Me Me Me — Me — Et racemic II-1096 Me Me Me — Me — Et (R)- II-1097 Me Me Me — Me — nPr racemic II-1098 Me Me Me — Me — nPr (R)- II-1099 Me Me Me — Me — iPr racemic II-1100 Me Me Me — Me — iPr (R)- II-1101 Me Me Me — Me — cPr racemic II-1102 Me Me Me — Me — cPr (R)- II-1103 Me Me Me — Me — cHex racemic II-1104 Me Me Me — Me — cHex (R)- II-1105 Me Me Me — Me — Ph racemic II-1106 Me Me Me — Me — Ph (R)- II-1107 Me Me Me — Me — 2-F—Ph racemic II-1108 Me Me Me — Me — 2-F—Ph (R)- II-1109 Me Me Me — Me — 3-F—Ph racemic II-1110 Me Me Me — Me — 3-F—Ph (R)- II-1111 Me Me Me — Me — 4-F—Ph racemic II-1112 Me Me Me — Me — 4-F—Ph (R)- II-1113 Me Me Me — Me — 2-Cl—Ph racemic II-1114 Me Me Me — Me — 2-Cl—Ph (R)- II-1115 Me Me Me — Me — 3-Cl—Ph racemic II-1116 Me Me Me — Me — 3-Cl—Ph (R)- II-1117 Me Me Me — Me — 4-Cl—Ph racemic II-1118 Me Me Me — Me — 4-Cl—Ph (R)- II-1119 Me Me Me — Me — 2-Py racemic II-1120 Me Me Me — Me — 2-Py (R)- II-1121 Me Me Me — Me — 3-Py racemic II-1122 Me Me Me — Me — 3-Py (R)- II-1123 Me Me Me — Me — 4-Py racemic II-1124 Me Me Me — Me — 4-Py (R)- II-1125 Me Me Me — iPr — H racemic II-1126 Me Me Me — iPr — H (R)-

TABLE 32 (II)

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration II-1127 Me Me Me — iPr — Me racemic II-1128 Me Me Me — iPr — Me (R)- II-1129 Me Me Me — iPr — CHF₂ racemic II-1130 Me Me Me — iPr — CHF₂ (R)- II-1131 Me Me Me — iPr — CF₃ racemic II-1132 Me Me Me — iPr — CF₃ (R)- II-1133 Me Me Me — iPr — Et racemic II-1134 Me Me Me — iPr — Et (R)- II-1135 Me Me Me — iPr — nPr racemic II-1136 Me Me Me — iPr — nPr (R)- II-1137 Me Me Me — iPr — iPr racemic II-1138 Me Me Me — iPr — iPr (R)- II-1139 Me Me Me — iPr — cPr racemic II-1140 Me Me Me — iPr — cPr (R)- II-1141 Me Me Me — iPr — Ph racemic II-1142 Me Me Me — iPr — Ph (R)- II-1143 Me Me Me — CF₃ — H racemic II-1144 Me Me Me — CF₃ — H (R)- II-1145 Me Me Me — CF₃ — Me racemic II-1146 Me Me Me — CF₃ — Me (R)- II-1147 Me Me Me — CF₃ — CHF₂ racemic II-1148 Me Me Me — CF₃ — CHF₂ (R)- II-1149 Me Me Me — CF₃ — CF₃ racemic II-1150 Me Me Me — CF₃ — CF₃ (R)- II-1151 Me Me Me — CF₃ — Et racemic II-1152 Me Me Me — CF₃ — Et (R)- II-1153 Me Me Me — CF₃ — nPr racemic II-1154 Me Me Me — CF₃ — nPr (R)- II-1155 Me Me Me — CF₃ — iPr racemic II-1156 Me Me Me — CF₃ — iPr (R)- II-1157 Me Me Me — CF₃ — cPr racemic II-1158 Me Me Me — CF₃ — cPr (R)- II-1159 Me Me Me — CF₃ — Ph racemic II-1160 Me Me Me — CF₃ — Ph (R)- II-1161 Me Me Me — CH₂OH — H racemic II-1162 Me Me Me — CH₂OH — H (R)- II-1163 Me Me Me — CH₂OH — Me racemic II-1164 Me Me Me — CH₂OH — Me (R)- II-1165 Me Me Me — CH₂OH — CHF₂ racemic II-1166 Me Me Me — CH₂OH — CHF₂ (R)- II-1167 Me Me Me — CH₂OH — CF₃ racemic II-1168 Me Me Me — CH₂OH — CF₃ (R)- II-1169 Me Me Me — CH₂OH — Et racemic II-1170 Me Me Me — CH₂OH — Et (R)- II-1171 Me Me Me — CH₂OH — nPr racemic II-1172 Me Me Me — CH₂OH — nPr (R)- II-1173 Me Me Me — CH₂OH — iPr racemic II-1174 Me Me Me — CH₂OH — iPr (R)- II-1175 Me Me Me — CH₂OH — cPr racemic II-1176 Me Me Me — CH₂OH — cPr (R)-

TABLE 33 (II)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration II-1177 Me Me Me — CH₂OH — Ph racemic II-1178 Me Me Me — CH₂OH — Ph (R)- II-1179 Me Me Me — CH₂OMe — H racemic II-1180 Me Me Me — CH₂OMe — H (R)- II-1181 Me Me Me — CH₂OMe — Me racemic II-1182 Me Me Me — CH₂OMe — Me (R)- II-1183 Me Me Me — CH₂OMe — CHF₂ racemic II-1184 Me Me Me — CH₂OMe — CHF₂ (R)- II-1185 Me Me Me — CH₂OMe — CF₃ racemic II-1186 Me Me Me — CH₂OMe — CF₃ (R)- II-1187 Me Me Me — CH₂OMe — Et racemic II-1188 Me Me Me — CH₂OMe — Et (R)- II-1189 Me Me Me — CH₂OMe — nPr racemic II-1190 Me Me Me — CH₂OMe — nPr (R)- II-1191 Me Me Me — CH₂OMe — iPr racemic II-1192 Me Me Me — CH₂OMe — iPr (R)- II-1193 Me Me Me — CH₂OMe — cPr racemic II-1194 Me Me Me — CH₂OMe — cPr (R)- II-1195 Me Me Me — CH₂OMe — Ph racemic II-1196 Me Me Me — CH₂OMe — Ph (R)- II-1197 Me Me Me — CH₂OBn — H racemic II-1198 Me Me Me — CH₂OBn — H (R)- II-1199 Me Me Me — CH₂OBn — Me racemic II-1200 Me Me Me — CH₂OBn — Me (R)- II-1201 Me Me Me — CH₂OBn — Ph racemic II-1202 Me Me Me — CH₂OBn — Ph (R)- II-1203 Me Me Me — CH₂NMe₂ — H racemic II-1204 Me Me Me — CH₂NMe₂ — H (R)- II-1205 Me Me Me — CH₂NMe₂ — Me racemic II-1206 Me Me Me — CH₂NMe₂ — Me (R)- II-1207 Me Me Me — CH₂NMe₂ — CHF₂ racemic II-1208 Me Me Me — CH₂NMe₂ — CHF₂ (R)- II-1209 Me Me Me — CH₂NMe₂ — CF₃ racemic II-1210 Me Me Me — CH₂NMe₂ — CF₃ (R)- II-1211 Me Me Me — CH₂NMe₂ — Et racemic II-1212 Me Me Me — CH₂NMe₂ — Et (R)- II-1213 Me Me Me — CH₂NMe₂ — nPr racemic II-1214 Me Me Me — CH₂NMe₂ — nPr (R)- II-1215 Me Me Me — CH₂NMe₂ — iPr racemic II-1216 Me Me Me — CH₂NMe₂ — iPr (R)- II-1217 Me Me Me — CH₂NMe₂ — cPr racemic II-1218 Me Me Me — CH₂NMe₂ — cPr (R)- II-1219 Me Me Me — CH₂NMe₂ — Ph racemic II-1220 Me Me Me — CH₂NMe₂ — Ph (R)- II-1221 Me Me Me — CH₂-(3,3- — H racemic difluoropyrrolidyl) II-1222 Me Me Me — CH₂-(3,3- — H (R)- difluoropyrrolidyl) II-1223 Me Me Me — CH₂-(3,3- — Me racemic difluoropyrrolidyl) II-1224 Me Me Me — CH₂-(3,3- — Me (R)- difluoropyrrolidyl) II-1225 Me Me Me — CH₂-(3,3- — Ph racemic difluoropyrrolidyl) II-1226 Me Me Me — CH₂-(3,3- — Ph (R)- difluoropyrrolidyl)

TABLE 34 (II)

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration II-1227 Me Me Me — 2-F—Ph — H racemic II-1228 Me Me Me — 2-F—Ph — H (R)- II-1229 Me Me Me — 2-F—Ph — Me racemic II-1230 Me Me Me — 2-F—Ph — Me (R)- II-1231 Me Me Me — 2-F—Ph — CHF₂ racemic II-1232 Me Me Me — 2-F—Ph — CHF₂ (R)- II-1233 Me Me Me — 2-F—Ph — CF₃ racemic II-1234 Me Me Me — 2-F—Ph — CF₃ (R)- II-1235 Me Me Me — 2-F—Ph — Et racemic II-1236 Me Me Me — 2-F—Ph — Et (R)- II-1237 Me Me Me — 2-F—Ph — nPr racemic II-1238 Me Me Me — 2-F—Ph — nPr (R)- II-1239 Me Me Me — 2-F—Ph — iPr racemic II-1240 Me Me Me — 2-F—Ph — iPr (R)- II-1241 Me Me Me — 2-F—Ph — cPr racemic II-1242 Me Me Me — 2-F—Ph — cPr (R)- II-1243 Me Me Me — 3-F—Ph — H racemic II-1244 Me Me Me — 3-F—Ph — H (R)- II-1245 Me Me Me — 3-F—Ph — Me racemic II-1246 Me Me Me — 3-F—Ph — Me (R)- II-1247 Me Me Me — 3-F—Ph — CHF₂ racemic II-1248 Me Me Me — 3-F—Ph — CHF₂ (R)- II-1249 Me Me Me — 3-F—Ph — CF₃ racemic II-1250 Me Me Me — 3-F—Ph — CF₃ (R)- II-1251 Me Me Me — 3-F—Ph — Et racemic II-1252 Me Me Me — 3-F—Ph — Et (R)- II-1253 Me Me Me — 3-F—Ph — nPr racemic II-1254 Me Me Me — 3-F—Ph — nPr (R)- II-1255 Me Me Me — 3-F—Ph — iPr racemic II-1256 Me Me Me — 3-F—Ph — iPr (R)- II-1257 Me Me Me — 3-F—Ph — cPr racemic II-1258 Me Me Me — 3-F—Ph — cPr (R)- II-1259 Me Me Me — 4-F—Ph — H racemic II-1260 Me Me Me — 4-F—Ph — H (R)- II-1261 Me Me Me — 4-F—Ph — Me racemic II-1262 Me Me Me — 4-F—Ph — Me (R)- II-1263 Me Me Me — 4-F—Ph — CHF₂ racemic II-1264 Me Me Me — 4-F—Ph — CHF₂ (R)- II-1265 Me Me Me — 4-F—Ph — CF₃ racemic II-1266 Me Me Me — 4-F—Ph — CF₃ (R)- II-1267 Me Me Me — 4-F—Ph — Et racemic II-1268 Me Me Me — 4-F—Ph — Et (R)- II-1269 Me Me Me — 4-F—Ph — nPr racemic II-1270 Me Me Me — 4-F—Ph — nPr (R)- II-1271 Me Me Me — 4-F—Ph — iPr racemic II-1272 Me Me Me — 4-F—Ph — iPr (R)- II-1273 Me Me Me — 4-F—Ph — cPr racemic II-1274 Me Me Me — 4-F—Ph — cPr (R)- II-1275 Me Me Me — 2-thienyl — H racemic II-1276 Me Me Me — 2-thienyl — H (S)-

TABLE 35 (II)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration II-1277 Me Me Me — 2-thienyl — Me racemic II-1278 Me Me Me — 2-thienyl — Me (S)- II-1279 Me Me Me — 2-thienyl — CHF₂ racemic II-1280 Me Me Me — 2-thienyl — CHF₂ (S)- II-1281 Me Me Me — 2-thienyl — CF₃ racemic II-1282 Me Me Me — 2-thienyl — CF₃ (S)- II-1283 Me Me Me — 2-thienyl — Et racemic II-1284 Me Me Me — 2-thienyl — Et (S)- II-1285 Me Me Me — 2-thienyl — nPr racemic II-1286 Me Me Me — 2-thienyl — nPr (S)- II-1287 Me Me Me — 2-thienyl — iPr racemic II-1288 Me Me Me — 2-thienyl — iPr (S)- II-1289 Me Me Me — 2-thienyl — cPr racemic II-1290 Me Me Me — 2-thienyl — cPr (S)- II-1291 Me Me Me — 3-thienyl — H racemic II-1292 Me Me Me — 3-thienyl — H (R)- II-1293 Me Me Me — 3-thienyl — Me racemic II-1294 Me Me Me — 3-thienyl — Me (R)- II-1295 Me Me Me — 3-thienyl — CHF₂ racemic II-1296 Me Me Me — 3-thienyl — CHF₂ (R)- II-1297 Me Me Me — 3-thienyl — CF₃ racemic II-1298 Me Me Me — 3-thienyl — CF₃ (R)- II-1299 Me Me Me — 3-thienyl — Et racemic II-1300 Me Me Me — 3-thienyl — Et (R)- II-1301 Me Me Me — 3-thienyl — nPr racemic II-1302 Me Me Me — 3-thienyl — nPr (R)- II-1303 Me Me Me — 3-thienyl — iPr racemic II-1304 Me Me Me — 3-thienyl — iPr (R)- II-1305 Me Me Me — 3-thienyl — cPr racemic II-1306 Me Me Me — 3-thienyl — cPr (R)-

TABLE 36 (III)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-1 Me Me Me O Ph CH₂ H racemic III-2 Me Me Me O Ph CH₂ H (S)- III-3 Me Et Me O Ph CH₂ H racemic III-4 Me Et Me O Ph CH₂ H (S)- III-5 Me Me Me O Ph CH₂ Me racemic III-6 Me Me Me O Ph CH₂ Me (S)- III-7 Me Et Me O Ph CH₂ Me racemic III-8 Me Et Me O Ph CH₂ Me (S)- III-9 Me Me Me O Ph CH₂ CHF₂ racemic III-10 Me Me Me O Ph CH₂ CHF₂ (S)- III-11 Me Et Me O Ph CH₂ CHF₂ racemic III-12 Me Et Me O Ph CH₂ CHF₂ (S)- III-13 Me Me Me O Ph CH₂ Et racemic III-14 Me Me Me O Ph CH₂ Et (S)- III-15 Me Et Me O Ph CH₂ Et racemic III-16 Me Et Me O Ph CH₂ Et (S)- III-17 Me Me Me O Ph CH₂ iPr racemic III-18 Me Me Me O Ph CH₂ iPr (S)- III-19 Me Et Me O Ph CH₂ iPr racemic III-20 Me Et Me O Ph CH₂ iPr (S)- III-21 Me Me Me O Ph CH₂ cPr racemic III-22 Me Me Me O Ph CH₂ cPr (S)- III-23 Me Et Me O Ph CH₂ cPr racemic III-24 Me Et Me O Ph CH₂ cPr (S)- III-25 Me Me Me O Ph CH₂ Ph racemic III-26 Me Me Me O Ph CH₂ Ph (S)- III-27 Me Et Me O Ph CH₂ Ph racemic III-28 Me Et Me O Ph CH₂ Ph (S)- III-29 Me Me Me O Ph C(Me)₂ H racemic III-30 Me Me Me O Ph C(Me)₂ H (S)- III-31 Me Et Me O Ph C(Me)₂ H racemic III-32 Me Et Me O Ph C(Me)₂ H (S)- III-33 Me Me Me O Ph C(Me)₂ Me racemic III-34 Me Me Me O Ph C(Me)₂ Me (S)- III-35 Me Et Me O Ph C(Me)₂ Me racemic III-36 Me Et Me O Ph C(Me)₂ Me (S)- III-37 Me Me Me O Ph C(Me)₂ CHF₂ racemic III-38 Me Me Me O Ph C(Me)₂ CHF₂ (S)- III-39 Me Et Me O Ph C(Me)₂ CHF₂ racemic III-40 Me Et Me O Ph C(Me)₂ CHF₂ (S)- III-41 Me Me Me O Ph C(Me)₂ Et racemic III-42 Me Me Me O Ph C(Me)₂ Et (S)- III-43 Me Et Me O Ph C(Me)₂ Et racemic III-44 Me Et Me O Ph C(Me)₂ Et (S)- III-45 Me Me Me O Ph C(Me)₂ iPr racemic III-46 Me Me Me O Ph C(Me)₂ iPr (S)- III-47 Me Et Me O Ph C(Me)₂ iPr racemic III-48 Me Et Me O Ph C(Me)₂ iPr (S)- III-49 Me Me Me O Ph C(Me)₂ cPr racemic III-50 Me Me Me O Ph C(Me)₂ cPr (S)-

TABLE 37 (III)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-51 Me Et Me O Ph C(Me)₂ cPr racemic III-52 Me Et Me O Ph C(Me)₂ cPr (S)- III-53 Me Me Me O Ph C(Me)₂ Ph racemic III-54 Me Me Me O Ph C(Me)₂ Ph (S)- III-55 Me Et Me O Ph C(Me)₂ Ph racemic III-56 Me Et Me O Ph C(Me)₂ Ph (S)- III-57 Me Me Me O Ph (CH₂)₂ H racemic III-58 Me Me Me O Ph (CH₂)₂ H (R)- III-59 Me Et Me O Ph (CH₂)₂ H racemic III-60 Me Et Me O Ph (CH₂)₂ H (R)- III-61 Me Me Me O Ph (CH₂)₂ Me racemic III-62 Me Me Me O Ph (CH₂)₂ Me (R)- III-63 Me Et Me O Ph (CH₂)₂ Me racemic III-64 Me Et Me O Ph (CH₂)₂ Me (R)- III-65 Me Me Me O Ph (CH₂)₂ CHF₂ racemic III-66 Me Me Me O Ph (CH₂)₂ CHF₂ (R)- III-67 Me Et Me O Ph (CH₂)₂ CHF₂ racemic III-68 Me Et Me O Ph (CH₂)₂ CHF₂ (R)- III-69 Me Me Me O Ph (CH₂)₂ Et racemic III-70 Me Me Me O Ph (CH₂)₂ Et (R)- III-71 Me Et Me O Ph (CH₂)₂ Et racemic III-72 Me Et Me O Ph (CH₂)₂ Et (R)- III-73 Me Me Me O Ph (CH₂)₂ iPr racemic III-74 Me Me Me O Ph (CH₂)₂ iPr (R)- III-75 Me Et Me O Ph (CH₂)₂ iPr racemic III-76 Me Et Me O Ph (CH₂)₂ iPr (R)- III-77 Me Me Me O Ph (CH₂)₂ cPr racemic III-78 Me Me Me O Ph (CH₂)₂ cPr (R)- III-79 Me Et Me O Ph (CH₂)₂ cPr racemic III-80 Me Et Me O Ph (CH₂)₂ cPr (R)- III-81 Me Me Me O Ph (CH₂)₂ Ph racemic III-82 Me Me Me O Ph (CH₂)₂ Ph (R)- III-83 Me Et Me O Ph (CH₂)₂ Ph racemic III-84 Me Et Me O Ph (CH₂)₂ Ph (R)- III-85 Me Me Me O Ph CH₂C(Me)₂ H racemic III-86 Me Me Me O Ph CH₂C(Me)₂ H (R)- III-87 Me Et Me O Ph CH₂C(Me)₂ H racemic III-88 Me Et Me O Ph CH₂C(Me)₂ H (R)- III-89 Me Me Me O Ph CH₂C(Me)₂ Me racemic III-90 Me Me Me O Ph CH₂C(Me)₂ Me (R)- III-91 Me Et Me O Ph CH₂C(Me)₂ Me racemic III-92 Me Et Me O Ph CH₂C(Me)₂ Me (R)- III-93 Me Me Me O Ph CH₂C(Me)₂ CHF₂ racemic III-94 Me Me Me O Ph CH₂C(Me)₂ CHF₂ (R)- III-95 Me Et Me O Ph CH₂C(Me)₂ CHF₂ racemic III-96 Me Et Me O Ph CH₂C(Me)₂ CHF₂ (R)- III-97 Me Me Me O Ph CH₂C(Me)₂ Et racemic III-98 Me Me Me O Ph CH₂C(Me)₂ Et (R)- III-99 Me Et Me O Ph CH₂C(Me)₂ Et racemic III-100 Me Et Me O Ph CH₂C(Me)₂ Et (R)-

TABLE 38 (III)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-101 Me Me Me O Ph CH₂C(Me)₂ iPr racemic III-102 Me Me Me O Ph CH₂C(Me)₂ iPr (R)- III-103 Me Et Me O Ph CH₂C(Me)₂ iPr racemic III-104 Me Et Me O Ph CH₂C(Me)₂ iPr (R)- III-105 Me Me Me O Ph CH₂C(Me)₂ cPr racemic III-106 Me Me Me O Ph CH₂C(Me)₂ cPr (R)- III-107 Me Et Me O Ph CH₂C(Me)₂ cPr racemic III-108 Me Et Me O Ph CH₂C(Me)₂ cPr (R)- III-109 Me Me Me O Ph CH₂C(Me)₂ Ph racemic III-110 Me Me Me O Ph CH₂C(Me)₂ Ph (R)- III-111 Me Et Me O Ph CH₂C(Me)₂ Ph racemic III-112 Me Et Me O Ph CH₂C(Me)₂ Ph (R)- III-113 Me Me Me NH Ph CH₂ H racemic III-114 Me Me Me NH Ph CH₂ H (S)- III-115 Me Et Me NH Ph CH₂ H racemic III-116 Me Et Me NH Ph CH₂ H (S)- III-117 Me Me Me N(Me) Ph CH₂ H racemic III-118 Me Me Me N(Me) Ph CH₂ H (S)- III-119 Me Et Me N(Me) Ph CH₂ H racemic III-120 Me Et Me N(Me) Ph CH₂ H (S)- III-121 Me Me Me NH Ph CH₂ Me racemic III-122 Me Me Me NH Ph CH₂ Me (S)- III-123 Me Et Me NH Ph CH₂ Me racemic III-124 Me Et Me NH Ph CH₂ Me (S)- III-125 Me Me Me N(Me) Ph CH₂ Me racemic III-126 Me Me Me N(Me) Ph CH₂ Me (S)- III-127 Me Et Me N(Me) Ph CH₂ Me racemic III-128 Me Et Me N(Me) Ph CH₂ Me (S)- III-129 Me Me Me NH Ph CH₂ CHF₂ racemic III-130 Me Me Me NH Ph CH₂ CHF₂ (S)- III-131 Me Et Me NH Ph CH₂ CHF₂ racemic III-132 Me Et Me NH Ph CH₂ CHF₂ (S)- III-133 Me Me Me N(Me) Ph CH₂ CHF₂ racemic III-134 Me Me Me N(Me) Ph CH₂ CHF₂ (S)- III-135 Me Et Me N(Me) Ph CH₂ CHF₂ racemic III-136 Me Et Me N(Me) Ph CH₂ CHF₂ (S)- III-137 Me Me Me NH Ph CH₂ Et racemic III-138 Me Me Me NH Ph CH₂ Et (S)- III-139 Me Et Me NH Ph CH₂ Et racemic III-140 Me Et Me NH Ph CH₂ Et (S)- III-141 Me Me Me N(Me) Ph CH₂ Et racemic III-142 Me Me Me N(Me) Ph CH₂ Et (S)- III-143 Me Et Me N(Me) Ph CH₂ Et racemic III-144 Me Et Me N(Me) Ph CH₂ Et (S)- III-145 Me Me Me NH Ph CH₂ iPr racemic III-146 Me Me Me NH Ph CH₂ iPr (S)- III-147 Me Et Me NH Ph CH₂ iPr racemic III-148 Me Et Me NH Ph CH₂ iPr (S)- III-149 Me Me Me N(Me) Ph CH₂ iPr racemic III-150 Me Me Me N(Me) Ph CH₂ iPr (S)-

TABLE 39 (III)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ guration III-151 Me Et Me N(Me) Ph CH₂ iPr racemic III-152 Me Et Me N(Me) Ph CH₂ iPr (S)- III-153 Me Me Me NH Ph CH₂ cPr racemic III-154 Me Me Me NH Ph CH₂ cPr (S)- III-155 Me Et Me NH Ph CH₂ cPr racemic III-156 Me Et Me NH Ph CH₂ cPr (S)- III-157 Me Me Me N(Me) Ph CH₂ cPr racemic III-158 Me Me Me N(Me) Ph CH₂ cPr (S)- III-159 Me Et Me N(Me) Ph CH₂ cPr racemic III-160 Me Et Me N(Me) Ph CH₂ cPr (S)- III-161 Me Me Me NH Ph CH₂ Ph racemic III-162 Me Me Me NH Ph CH₂ Ph (S)- III-163 Me Et Me NH Ph CH₂ Ph racemic III-164 Me Et Me NH Ph CH₂ Ph (S)- III-165 Me Me Me N(Me) Ph CH₂ Ph racemic III-166 Me Me Me N(Me) Ph CH₂ Ph (S)- III-167 Me Et Me N(Me) Ph CH₂ Ph racemic III-168 Me Et Me N(Me) Ph CH₂ Ph (S)- III-169 Me Me Me NH Ph C(Me)₂ H racemic III-170 Me Me Me NH Ph C(Me)₂ H (S)- III-171 Me Et Me NH Ph C(Me)₂ H racemic III-172 Me Et Me NH Ph C(Me)₂ H (S)- III-173 Me Me Me N(Me) Ph C(Me)₂ H racemic III-174 Me Me Me N(Me) Ph C(Me)₂ H (S)- III-175 Me Et Me N(Me) Ph C(Me)₂ H racemic III-176 Me Et Me N(Me) Ph C(Me)₂ H (S)- III-177 Me Me Me NH Ph C(Me)₂ Me racemic III-178 Me Me Me NH Ph C(Me)₂ Me (S)- III-179 Me Et Me NH Ph C(Me)₂ Me racemic III-180 Me Et Me NH Ph C(Me)₂ Me (S)- III-181 Me Me Me N(Me) Ph C(Me)₂ Me racemic III-182 Me Me Me N(Me) Ph C(Me)₂ Me (S)- III-183 Me Et Me N(Me) Ph C(Me)₂ Me racemic III-184 Me Et Me N(Me) Ph C(Me)₂ Me (S)- III-185 Me Me Me NH Ph C(Me)₂ CHF₂ racemic III-186 Me Me Me NH Ph C(Me)₂ CHF₂ (S)- III-187 Me Et Me NH Ph C(Me)₂ CHF₂ racemic III-188 Me Et Me NH Ph C(Me)₂ CHF₂ (S)- III-189 Me Me Me N(Me) Ph C(Me)₂ CHF₂ racemic III-190 Me Me Me N(Me) Ph C(Me)₂ CHF₂ (S)- III-191 Me Et Me N(Me) Ph C(Me)₂ CHF₂ racemic III-192 Me Et Me N(Me) Ph C(Me)₂ CHF₂ (S)- III-193 Me Me Me NH Ph C(Me)₂ Et racemic III-194 Me Me Me NH Ph C(Me)₂ Et (S)- III-195 Me Et Me NH Ph C(Me)₂ Et racemic III-196 Me Et Me NH Ph C(Me)₂ Et (S)- III-197 Me Me Me N(Me) Ph C(Me)₂ Et racemic III-198 Me Me Me N(Me) Ph C(Me)₂ Et (S)- III-199 Me Et Me N(Me) Ph C(Me)₂ Et racemic III-200 Me Et Me N(Me) Ph C(Me)₂ Et (S)-

TABLE 40 (III)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-201 Me Me Me NH Ph C(Me)₂ iPr racemic III-202 Me Me Me NH Ph C(Me)₂ iPr (S)- III-203 Me Et Me NH Ph C(Me)₂ iPr racemic III-204 Me Et Me NH Ph C(Me)₂ iPr (S)- III-205 Me Me Me N(Me) Ph C(Me)₂ iPr racemic III-206 Me Me Me N(Me) Ph C(Me)₂ iPr (S)- III-207 Me Et Me N(Me) Ph C(Me)₂ iPr racemic III-208 Me Et Me N(Me) Ph C(Me)₂ iPr (S)- III-209 Me Me Me NH Ph C(Me)₂ cPr racemic III-210 Me Me Me NH Ph C(Me)₂ cPr (S)- III-211 Me Et Me NH Ph C(Me)₂ cPr racemic III-212 Me Et Me NH Ph C(Me)₂ cPr (S)- III-213 Me Me Me N(Me) Ph C(Me)₂ cPr racemic III-214 Me Me Me N(Me) Ph C(Me)₂ cPr (S)- III-215 Me Et Me N(Me) Ph C(Me)₂ cPr racemic III-216 Me Et Me N(Me) Ph C(Me)₂ cPr (S)- III-217 Me Me Me NH Ph C(Me)₂ Ph racemic III-218 Me Me Me NH Ph C(Me)₂ Ph (S)- III-219 Me Et Me NH Ph C(Me)₂ Ph racemic III-220 Me Et Me NH Ph C(Me)₂ Ph (S)- III-221 Me Me Me N(Me) Ph C(Me)₂ Ph racemic III-222 Me Me Me N(Me) Ph C(Me)₂ Ph (S)- III-223 Me Et Me N(Me) Ph C(Me)₂ Ph racemic III-224 Me Et Me N(Me) Ph C(Me)₂ Ph (S)- III-225 Me Me Me NH Ph C(Me)₂ H racemic III-226 Me Me Me NH Ph C(Me)₂ H (R)- III-227 Me Et Me NH Ph C(Me)₂ H racemic III-228 Me Et Me NH Ph C(Me)₂ H (R)- III-229 Me Me Me N(Me) Ph C(Me)₂ H racemic III-230 Me Me Me N(Me) Ph C(Me)₂ H (R)- III-231 Me Et Me N(Me) Ph C(Me)₂ H racemic III-232 Me Et Me N(Me) Ph C(Me)₂ H (R)- III-233 Me Me Me NH Ph C(Me)₂ Me racemic III-234 Me Me Me NH Ph C(Me)₂ Me (R)- III-235 Me Et Me NH Ph C(Me)₂ Me racemic III-236 Me Et Me NH Ph C(Me)₂ Me (R)- III-237 Me Me Me N(Me) Ph C(Me)₂ Me racemic III-238 Me Me Me N(Me) Ph C(Me)₂ Me (R)- III-239 Me Et Me N(Me) Ph C(Me)₂ Me racemic III-240 Me Et Me N(Me) Ph C(Me)₂ Me (R)- III-241 Me Me Me NH Ph C(Me)₂ CHF₂ racemic III-242 Me Me Me NH Ph C(Me)₂ CHF₂ (R)- III-243 Me Et Me NH Ph C(Me)₂ CHF₂ racemic III-244 Me Et Me NH Ph C(Me)₂ CHF₂ (R)- III-245 Me Me Me N(Me) Ph C(Me)₂ CHF₂ racemic III-246 Me Me Me N(Me) Ph C(Me)₂ CHF₂ (R)- III-247 Me Et Me N(Me) Ph C(Me)₂ CHF₂ racemic III-248 Me Et Me N(Me) Ph C(Me)₂ CHF₂ (R)- III-249 Me Me Me NH Ph C(Me)₂ Et racemic III-250 Me Me Me NH Ph C(Me)₂ Et (R)-

TABLE 41

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration III-251 Me Et Me NH Ph (CH₂)₂ Et racemic III-252 Me Et Me NH Ph (CH₂)₂ Et (R)- III-253 Me Me Me N(Me) Ph (CH₂)₂ Et racemic III-254 Me Me Me N(Me) Ph (CH₂)₂ Et (R)- III-255 Me Et Me N(Me) Ph (CH₂)₂ Et racemic III-256 Me Et Me N(Me) Ph (CH₂)₂ Et (R)- III-257 Me Me Me NH Ph (CH₂)₂ iPr racemic III-258 Me Me Me NH Ph (CH₂)₂ iPr (R)- III-259 Me Et Me NH Ph (CH₂)₂ iPr racemic III-260 Me Et Me NH Ph (CH₂)₂ iPr (R)- III-261 Me Me Me N(Me) Ph (CH₂)₂ iPr racemic III-262 Me Me Me N(Me) Ph (CH₂)₂ iPr (R)- III-263 Me Et Me N(Me) Ph (CH₂)₂ iPr racemic III-264 Me Et Me N(Me) Ph (CH₂)₂ iPr (R)- III-265 Me Me Me NH Ph (CH₂)₂ cPr racemic III-266 Me Me Me NH Ph (CH₂)₂ cPr (R)- III-267 Me Et Me NH Ph (CH₂)₂ cPr racemic III-268 Me Et Me NH Ph (CH₂)₂ cPr (R)- III-269 Me Me Me N(Me) Ph (CH₂)₂ cPr racemic III-270 Me Me Me N(Me) Ph (CH₂)₂ cPr (R)- III-271 Me Et Me N(Me) Ph (CH₂)₂ cPr racemic III-272 Me Et Me N(Me) Ph (CH₂)₂ cPr (R)- III-273 Me Me Me NH Ph (CH₂)₂ Ph racemic III-274 Me Me Me NH Ph (CH₂)₂ Ph (R)- III-275 Me Et Me NH Ph (CH₂)₂ Ph racemic III-276 Me Et Me NH Ph (CH₂)₂ Ph (R)- III-277 Me Me Me N(Me) Ph (CH₂)₂ Ph racemic III-278 Me Me Me N(Me) Ph (CH₂)₂ Ph (R)- III-279 Me Et Me N(Me) Ph (CH₂)₂ Ph racemic III-280 Me Et Me N(Me) Ph (CH₂)₂ Ph (R)- III-281 Me Me Me NH Ph (CH₂)₃ H racemic III-282 Me Me Me NH Ph (CH₂)₃ H (R)- III-283 Me Et Me NH Ph (CH₂)₃ H racemic III-284 Me Et Me NH Ph (CH₂)₃ H (R)- III-285 Me Me Me N(Me) Ph (CH₂)₃ H racemic III-286 Me Me Me N(Me) Ph (CH₂)₃ H (R)- III-287 Me Et Me N(Me) Ph (CH₂)₃ H racemic III-288 Me Et Me N(Me) Ph (CH₂)₃ H (R)- III-289 Me Me Me NH Ph (CH₂)₄ H racemic III-290 Me Me Me NH Ph (CH₂)₄ H (R)- III-291 Me Et Me NH Ph (CH₂)₄ H racemic III-292 Me Et Me NH Ph (CH₂)₄ H (R)- III-293 Me Me Me N(Me) Ph (CH₂)₄ H racemic III-294 Me Me Me N(Me) Ph (CH₂)₄ H (R)- III-295 Me Et Me N(Me) Ph (CH₂)₄ H racemic III-296 Me Et Me N(Me) Ph (CH₂)₄ H (R)- III-297 Me Me Me NH Ph CH₂C(Me)₂ H racemic III-298 Me Me Me NH Ph CH₂C(Me)₂ H (R)- III-299 Me Et Me NH Ph CH₂C(Me)₂ H racemic III-300 Me Et Me NH Ph CH₂C(Me)₂ H (R)-

TABLE 42

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration III-301 Me Me Me N(Me) Ph CH₂C(Me)₂ H racemic III-302 Me Me Me N(Me) Ph CH₂C(Me)₂ H (R)- III-303 Me Et Me N(Me) Ph CH₂C(Me)₂ H racemic III-304 Me Et Me N(Me) Ph CH₂C(Me)₂ H (R)- III-305 Me Me Me NH Ph CH₂C(Me)₂ Me racemic III-306 Me Me Me NH Ph CH₂C(Me)₂ Me (R)- III-307 Me Et Me NH Ph CH₂C(Me)₂ Me racemic III-308 Me Et Me NH Ph CH₂C(Me)₂ Me (R)- III-309 Me Me Me N(Me) Ph CH₂C(Me)₂ Me racemic III-310 Me Me Me N(Me) Ph CH₂C(Me)₂ Me (R)- III-311 Me Et Me N(Me) Ph CH₂C(Me)₂ Me racemic III-312 Me Et Me N(Me) Ph CH₂C(Me)₂ Me (R)- III-313 Me Me Me NH Ph CH₂C(Me)₂ CHF₂ racemic III-314 Me Me Me NH Ph CH₂C(Me)₂ CHF₂ (R)- III-315 Me Et Me NH Ph CH₂C(Me)₂ CHF₂ racemic III-316 Me Et Me NH Ph CH₂C(Me)₂ CHF₂ (R)- III-317 Me Me Me N(Me) Ph CH₂C(Me)₂ CHF₂ racemic III-318 Me Me Me N(Me) Ph CH₂C(Me)₂ CHF₂ (R)- III-319 Me Et Me N(Me) Ph CH₂C(Me)₂ CHF₂ racemic III-320 Me Et Me N(Me) Ph CH₂C(Me)₂ CHF₂ (R)- III-321 Me Me Me NH Ph CH₂C(Me)₂ Et racemic III-322 Me Me Me NH Ph CH₂C(Me)₂ Et (R)- III-323 Me Et Me NH Ph CH₂C(Me)₂ Et racemic III-324 Me Et Me NH Ph CH₂C(Me)₂ Et (R)- III-325 Me Me Me N(Me) Ph CH₂C(Me)₂ Et racemic III-326 Me Me Me N(Me) Ph CH₂C(Me)₂ Et (R)- III-327 Me Et Me N(Me) Ph CH₂C(Me)₂ Et racemic III-328 Me Et Me N(Me) Ph CH₂C(Me)₂ Et (R)- III-329 Me Me Me NH Ph CH₂C(Me)₂ iPr racemic III-330 Me Me Me NH Ph CH₂C(Me)₂ iPr (R)- III-331 Me Et Me NH Ph CH₂C(Me)₂ iPr racemic III-332 Me Et Me NH Ph CH₂C(Me)₂ iPr (R)- III-333 Me Me Me N(Me) Ph CH₂C(Me)₂ iPr racemic III-334 Me Me Me N(Me) Ph CH₂C(Me)₂ iPr (R)- III-335 Me Et Me N(Me) Ph CH₂C(Me)₂ iPr racemic III-336 Me Et Me N(Me) Ph CH₂C(Me)₂ iPr (R)- III-337 Me Me Me NH Ph CH₂C(Me)₂ cPr racemic III-338 Me Me Me NH Ph CH₂C(Me)₂ cPr (R)- III-339 Me Et Me NH Ph CH₂C(Me)₂ cPr racemic III-340 Me Et Me NH Ph CH₂C(Me)₂ cPr (R)- III-341 Me Me Me N(Me) Ph CH₂C(Me)₂ cPr racemic III-342 Me Me Me N(Me) Ph CH₂C(Me)₂ cPr (R)- III-343 Me Et Me N(Me) Ph CH₂C(Me)₂ cPr racemic III-344 Me Et Me N(Me) Ph CH₂C(Me)₂ cPr (R)- III-345 Me Me Me NH Ph CH₂C(Me)₂ Ph racemic III-346 Me Me Me NH Ph CH₂C(Me)₂ Ph (R)- III-347 Me Et Me NH Ph CH₂C(Me)₂ Ph racemic III-348 Me Et Me NH Ph CH₂C(Me)₂ Ph (R)- III-349 Me Me Me N(Me) Ph CH₂C(Me)₂ Ph racemic III-350 Me Me Me N(Me) Ph CH₂C(Me)₂ Ph (R)-

TABLE 43

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration III-351 Me Et Me N(Me) Ph CH₂C(Me)₂ Ph racemic III-352 Me Et Me N(Me) Ph CH₂C(Me)₂ Ph (R)- III-353 Me Me Me NH Ph CH₂C(Me)₂ H racemic III-354 Me Me Me NH Ph CH₂C(Me)₂ H (S)- III-355 Me Et Me NH Ph CH₂C(Me)₂ H racemic III-356 Me Et Me NH Ph CH₂C(Me)₂ H (S)- III-357 Me Me Me N(Me) Ph CH₂C(Me)₂ H racemic III-358 Me Me Me N(Me) Ph CH₂C(Me)₂ H (S)- III-359 Me Et Me N(Me) Ph CH₂C(Me)₂ H racemic III-360 Me Et Me N(Me) Ph CH₂C(Me)₂ H (S)- III-361 Me Me Me NH Ph CF₂CH₂ H racemic III-362 Me Me Me NH Ph CF₂CH₂ H (S)- III-363 Me Et Me NH Ph CF₂CH₂ H racemic III-364 Me Et Me NH Ph CF₂CH₂ H (S)- III-365 Me Me Me N(Me) Ph CF₂CH₂ H racemic III-366 Me Me Me N(Me) Ph CF₂CH₂ H (S)- III-367 Me Et Me N(Me) Ph CF₂CH₂ H racemic III-368 Me Et Me N(Me) Ph CF₂CH₂ H (S)- III-369 Me Me Me NH Ph CH═CHCH₂ H racemic III-370 Me Me Me NH Ph CH═CHCH₂ H (S)- III-371 Me Et Me NH Ph CH═CHCH₂ H racemic III-372 Me Et Me NH Ph CH═CHCH₂ H (S)- III-373 Me Me Me N(Me) Ph CH═CHCH₂ H racemic III-374 Me Me Me N(Me) Ph CH═CHCH₂ H (S)- III-375 Me Et Me N(Me) Ph CH═CHCH₂ H racemic III-376 Me Et Me N(Me) Ph CH═CHCH₂ H (S)- III-377 Me Me Me NH Ph C═CCH₂ H racemic III-378 Me Me Me NH Ph C═CCH₂ H (S)- III-379 Me Et Me NH Ph C═CCH₂ H racemic III-380 Me Et Me NH Ph C═CCH₂ H (S)- III-381 Me Me Me N(Me) Ph C═CCH₂ H racemic III-382 Me Me Me N(Me) Ph C═CCH₂ H (S)- III-383 Me Et Me N(Me) Ph C═CCH₂ H racemic III-384 Me Et Me N(Me) Ph C═CCH₂ H (S)- III-385 Me Me Me NH Ph 1,1-Cyclopropylene H racemic III-386 Me Me Me NH Ph 1,1-Cyclopropylene H (S)- III-387 Me Et Me NH Ph 1,1-Cyclopropylene H racemic III-388 Me Et Me NH Ph 1,1-Cyclopropylene H (S)- III-389 Me Me Me N(Me) Ph 1,1-Cyclopropylene H racemic III-390 Me Me Me N(Me) Ph 1,1-Cyclopropylene H (S)- III-391 Me Et Me N(Me) Ph 1,1-Cyclopropylene H racemic III-392 Me Et Me N(Me) Ph 1,1-Cyclopropylene H (S)- III-393 Me Me Me NH Ph 1,2-Cyclopropylene H racemic III-394 Me Me Me NH Ph 1,2-Cyclopropylene H (S)- III-395 Me Et Me NH Ph 1,2-Cyclopropylene H racemic III-396 Me Et Me NH Ph 1,2-Cyclopropylene H (S)- III-397 Me Me Me N(Me) Ph 1,2-Cyclopropylene H racemic III-398 Me Me Me N(Me) Ph 1,2-Cyclopropylene H (S)- III-399 Me Et Me N(Me) Ph 1,2-Cyclopropylene H racemic III-400 Me Et Me N(Me) Ph 1,2-Cyclopropylene H (S)-

TABLE 44

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration III-401 Me Me Me NH Ph C(═O) H racemic III-402 Me Me Me NH Ph C(═O) H (S)- III-403 Me Et Me NH Ph C(═O) H racemic III-404 Me Et Me NH Ph C(═O) H (S)- III-405 Me Me Me N(Me) Ph C(═O) H racemic III-406 Me Me Me N(Me) Ph C(═O) H (S)- III-407 Me Et Me N(Me) Ph C(═O) H racemic III-408 Me Et Me N(Me) Ph C(═O) H (S)- III-409 Me Me Me NH Ph C(═O) Bn racemic III-410 Me Me Me NH Ph C(═O) Bn (S)- III-411 Me Et Me NH Ph C(═O) Bn racemic III-412 Me Et Me NH Ph C(═O) Bn (S)- III-413 Me Me Me N(Me) Ph C(═O) Bn racemic III-414 Me Me Me N(Me) Ph C(═O) Bn (S)- III-415 Me Et Me N(Me) Ph C(═O) Bn racemic III-416 Me Et Me N(Me) Ph C(═O) Bn (S)- III-417 Me Me Me NH Ph C(═O) Me racemic III-418 Me Me Me NH Ph C(═O) Me (S)- III-419 Me Et Me NH Ph C(═O) Me racemic III-420 Me Et Me NH Ph C(═O) Me (S)- III-421 Me Me Me N(Me) Ph C(═O) Me racemic III-422 Me Me Me N(Me) Ph C(═O) Me (S)- III-423 Me Et Me N(Me) Ph C(═O) Me racemic III-424 Me Et Me N(Me) Ph C(═O) Me (S)- III-425 Me Me Me NH H CH₂ H III-426 Me Et Me NH H CH₂ H III-427 Me Me Me N(Me) H CH₂ H III-428 Me Et Me N(Me) H CH₂ H III-429 Me Me Me NH H CH(Me) H III-430 Me Et Me NH H CH(Me) H III-431 Me Me Me N(Me) H CH(Me) H III-432 Me Et Me N(Me) H CH(Me) H III-433 Me Me Me NH H CH(iPr) H III-434 Me Et Me NH H CH(iPr) H III-435 Me Me Me N(Me) H CH(iPr) H III-436 Me Et Me N(Me) H CH(iPr) H III-437 Me Me Me NH H CH(Ph) H III-438 Me Et Me NH H CH(Ph) H III-439 Me Me Me N(Me) H CH(Ph) H III-440 Me Et Me N(Me) H CH(Ph) H III-441 Me Me Me NH Me CH₂ H racemic III-442 Me Me Me NH Me CH₂ H (S)- III-443 Me Et Me NH Me CH₂ H racemic III-444 Me Et Me NH Me CH₂ H (S)- III-445 Me Me Me N(Me) Me CH₂ H racemic III-446 Me Me Me N(Me) Me CH₂ H (S)- III-447 Me Et Me N(Me) Me CH₂ H racemic III-448 Me Et Me N(Me) Me CH₂ H (S)- III-449 Me Me Me NH iPr CH₂ H racemic III-450 Me Me Me NH iPr CH₂ H (S)-

TABLE 45

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration III-451 Me Et Me NH iPr CH₂ H racemic III-452 Me Et Me NH iPr CH₂ H (S)- III-453 Me Me Me N(Me) iPr CH₂ H racemic III-454 Me Me Me N(Me) iPr CH₂ H (S)- III-455 Me Et Me N(Me) iPr CH₂ H racemic III-456 Me Et Me N(Me) iPr CH₂ H (S)- III-457 Me Me Me NH cHex CH₂ H racemic III-458 Me Me Me NH cHex CH₂ H (S)- III-459 Me Et Me NH cHex CH₂ H racemic III-460 Me Et Me NH cHex CH₂ H (S)- III-461 Me Me Me N(Me) cHex CH₂ H racemic III-462 Me Me Me N(Me) cHex CH₂ H (S)- III-463 Me Et Me N(Me) cHex CH₂ H racemic III-464 Me Et Me N(Me) cHex CH₂ H (S)- III-465 Me Me Me NH 1,3-Benzodioxol-4-yl CH₂ H racemic III-466 Me Me Me NH 1,3-Benzodioxol-4-yl CH₂ H (S)- III-467 Me Et Me NH 1,3-Benzodioxol-4-yl CH₂ H racemic III-468 Me Et Me NH 1,3-Benzodioxol-4-yl CH₂ H (S)- III-469 Me Me Me N(Me) 1,3-Benzodioxol-4-yl CH₂ H racemic III-470 Me Me Me N(Me) 1,3-Benzodioxol-4-yl CH₂ H (S)- III-471 Me Et Me N(Me) 1,3-Benzodioxol-4-yl CH₂ H racemic III-472 Me Et Me N(Me) 1,3-Benzodioxol-4-yl CH₂ H (S)- III-473 Me Me Me NH 2-F-Ph CH₂ H racemic III-474 Me Me Me NH 2-F-Ph CH₂ H (S)- III-475 Me Et Me NH 2-F-Ph CH₂ H racemic III-476 Me Et Me NH 2-F-Ph CH₂ H (S)- III-477 Me Me Me N(Me) 2-F-Ph CH₂ H racemic III-478 Me Me Me N(Me) 2-F-Ph CH₂ H (S)- III-479 Me Et Me N(Me) 2-F-Ph CH₂ H racemic III-480 Me Et Me N(Me) 2-F-Ph CH₂ H (S)- III-481 Me Me Me NH 3-F-Ph CH₂ H racemic III-482 Me Me Me NH 3-F-Ph CH₂ H (S)- III-483 Me Et Me NH 3-F-Ph CH₂ H racemic III-484 Me Et Me NH 3-F-Ph CH₂ H (S)- III-485 Me Me Me N(Me) 3-F-Ph CH₂ H racemic III-486 Me Me Me N(Me) 3-F-Ph CH₂ H (S)- III-487 Me Et Me N(Me) 3-F-Ph CH₂ H racemic III-488 Me Et Me N(Me) 3-F-Ph CH₂ H (S)- III-489 Me Me Me NH 4-F-Ph CH₂ H racemic III-490 Me Me Me NH 4-F-Ph CH₂ H (S)- III-491 Me Et Me NH 4-F-Ph CH₂ H racemic III-492 Me Et Me NH 4-F-Ph CH₂ H (S)- III-493 Me Me Me N(Me) 4-F-Ph CH₂ H racemic III-494 Me Me Me N(Me) 4-F-Ph CH₂ H (S)- III-495 Me Et Me N(Me) 4-F-Ph CH₂ H racemic III-496 Me Et Me N(Me) 4-F-Ph CH₂ H (S)- III-497 Me Me Me NH 2-Py CH₂ H racemic III-498 Me Me Me NH 2-Py CH₂ H (S)- III-499 Me Et Me NH 2-Py CH₂ H racemic III-500 Me Et Me NH 2-Py CH₂ H (S)-

TABLE 46

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration III-501 Me Me Me N(Me) 2-Py CH₂ H racemic III-502 Me Me Me N(Me) 2-Py CH₂ H (S)- III-503 Me Et Me N(Me) 2-Py CH₂ H racemic III-504 Me Et Me N(Me) 2-Py CH₂ H (S)- III-505 Me Me Me NH 3-Py CH₂ H racemic III-506 Me Me Me NH 3-Py CH₂ H (S)- III-507 Me Et Me NH 3-Py CH₂ H racemic III-508 Me Et Me NH 3-Py CH₂ H (S)- III-509 Me Me Me N(Me) 3-Py CH₂ H racemic III-510 Me Me Me N(Me) 3-Py CH₂ H (S)- III-511 Me Et Me N(Me) 3-Py CH₂ H racemic III-512 Me Et Me N(Me) 3-Py CH₂ H (S)- III-513 Me Me Me NH 4-Py CH₂ H racemic III-514 Me Me Me NH 4-Py CH₂ H (S)- III-515 Me Et Me NH 4-Py CH₂ H racemic III-516 Me Et Me NH 4-Py CH₂ H (S)- III-517 Me Me Me N(Me) 4-Py CH₂ H racemic III-518 Me Me Me N(Me) 4-Py CH₂ H (S)- III-519 Me Et Me N(Me) 4-Py CH₂ H racemic III-520 Me Et Me N(Me) 4-Py CH₂ H (S)- III-521 Me Me Me CH₂ Ph CH₂ H racemic III-522 Me Me Me CH₂ Ph CH₂ H (S)- III-523 Me Et Me CH₂ Ph CH₂ H racemic III-524 Me Et Me CH₂ Ph CH₂ H (S)- III-525 Me Me Me CH₂ Ph — H racemic III-526 Me Me Me CH₂ Ph — H (S)- III-527 Me Et Me CH₂ Ph — H racemic III-528 Me Et Me CH₂ Ph — H (S)- III-529 Me Me Me CH₂ Ph CH₂ Me racemic III-530 Me Me Me CH₂ Ph CH₂ Me (S)- III-531 Me Et Me CH₂ Ph CH₂ Me racemic III-532 Me Et Me CH₂ Ph CH₂ Me (S)- III-533 Me Me Me CH₂ Ph CH₂ CHF2 racemic III-534 Me Me Me CH₂ Ph CH₂ CHF2 (S)- III-535 Me Et Me CH₂ Ph CH₂ CHF2 racemic III-536 Me Et Me CH₂ Ph CH₂ CHF2 (S)- III-537 Me Me Me CH₂ Ph CH₂ Et racemic III-538 Me Me Me CH₂ Ph CH₂ Et (S)- III-539 Me Et Me CH₂ Ph CH₂ Et racemic III-540 Me Et Me CH₂ Ph CH₂ Et (S)- III-541 Me Me Me CH₂ Ph CH₂ cPr racemic III-542 Me Me Me CH₂ Ph CH₂ cPr (S)- III-543 Me Me Me CH₂ Ph CH₂ Ph racemic III-544 Me Me Me CH₂ Ph CH₂ Ph (S)- III-545 Me Me Me CH₂ Ph C(Me)₂ H racemic III-546 Me Me Me CH₂ Ph C(Me)₂ H (S)- III-547 Me Et Me CH₂ Ph C(Me)₂ H racemic III-548 Me Et Me CH₂ Ph C(Me)₂ H (S)- III-549 Me Me Me CH₂ Ph C(Me)₂ Me racemic III-550 Me Me Me CH₂ Ph C(Me)₂ Me (S)-

TABLE 47

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration III-551 Me Et Me CH₂ Ph C(Me)₂ Me racemic III-552 Me Et Me CH₂ Ph C(Me)₂ Me (S)- III-553 Me Me Me CH₂ Ph C(Me)₂ CHF₂ racemic III-554 Me Me Me CH₂ Ph C(Me)₂ CHF₂ (S)- III-555 Me Me Me CH₂ Ph C(Me)₂ Et racemic III-556 Me Me Me CH₂ Ph C(Me)₂ Et (S)- III-557 Me Me Me CH₂ Ph C(Me)₂ cPr racemic III-558 Me Me Me CH₂ Ph C(Me)₂ cPr (S)- III-559 Me Me Me CH₂ Ph C(Me)₂ Ph racemic III-560 Me Me Me CH₂ Ph C(Me)₂ Ph (S)- III-561 Me Me Me CH₂ Ph (CH₂)₂ H racemic III-562 Me Me Me CH₂ Ph (CH₂)₂ H (S)- III-563 Me Et Me CH₂ Ph (CH₂)₂ H racemic III-564 Me Et Me CH₂ Ph (CH₂)₂ H (S)- III-565 Me Me Me CH₂ Ph (CH₂)₂ Me racemic III-566 Me Me Me CH₂ Ph (CH₂)₂ Me (S)- III-567 Me Me Me CH₂ Ph (CH₂)₂ CHF₂ racemic III-568 Me Me Me CH₂ Ph (CH₂)₂ CHF₂ (S)- III-569 Me Me Me CH₂ Ph (CH₂)₂ Et racemic III-570 Me Me Me CH₂ Ph (CH₂)₂ Et (S)- III-571 Me Me Me CH₂ Ph (CH₂)₂ cPr racemic III-572 Me Me Me CH₂ Ph (CH₂)₂ cPr (S)- III-573 Me Me Me CH₂ Ph (CH₂)₂ Ph racemic III-574 Me Me Me CH₂ Ph (CH₂)₂ Ph (S)- III-575 Me Me Me CH₂ Ph CH₂C(Me)₂ H racemic III-576 Me Me Me CH₂ Ph CH₂C(Me)₂ H (S)- III-577 Me Et Me CH₂ Ph CH₂C(Me)₂ H racemic III-578 Me Et Me CH₂ Ph CH₂C(Me)₂ H (S)- III-579 Me Me Me CH₂ Ph CH₂C(Me)₂ Me racemic III-580 Me Me Me CH₂ Ph CH₂C(Me)₂ Me (S)- III-581 Me Et Me CH₂ Ph CH₂C(Me)₂ Me racemic III-582 Me Et Me CH₂ Ph CH₂C(Me)₂ Me (S)- III-583 Me Me Me CH₂ Ph CH₂C(Me)₂ CHF₂ racemic III-584 Me Me Me CH₂ Ph CH₂C(Me)₂ CHF₂ (S)- III-585 Me Me Me CH₂ Ph CH₂C(Me)₂ Et racemic III-586 Me Me Me CH₂ Ph CH₂C(Me)₂ Et (S)- III-587 Me Me Me CH₂ Ph CH₂C(Me)₂ cPr racemic III-588 Me Me Me CH₂ Ph CH₂C(Me)₂ cPr (S)- III-589 Me Me Me CH₂ Ph CH₂C(Me)₂ Ph racemic III-590 Me Me Me CH₂ Ph CH₂C(Me)₂ Ph (S)- III-591 Me Me Me — Ph CH₂ H racemic III-592 Me Me Me — Ph CH₂ H (S)- III-593 Me Me Me — Ph CH₂ Me racemic III-594 Me Me Me — Ph CH₂ Me (S)- III-595 Me Me Me CH═CH Ph CH₂ H racemic III-596 Me Me Me CH═CH Ph CH₂ H (S)- III-597 Me Me Me CH═CH Ph CH₂ Me racemic III-598 Me Me Me CH═CH Ph CH₂ Me (S)- III-599 Me Me Me C═C Ph CH₂ H racemic III-600 Me Me Me C═C Ph CH₂ H (S)-

TABLE 48

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration III-601 Me Me Me C═C Ph CH₂ Me racemic III-602 Me Me Me C═C Ph CH₂ Me (S)- III-603 Me Me Me 1,2-Cyclopropylene Ph CH₂ H racemic III-604 Me Me Me 1,2-Cyclopropylene Ph CH₂ H (S)- III-605 Me Me Me 1,2-Cyclopropylene Ph CH₂ Me racemic III-606 Me Me Me 1,2-Cyclopropylene Ph CH₂ Me (S)- III-607 Me Me Me 1,2-Cyclopropylene Ph CH₂ H racemic III-608 Me Me Me 1,2-Cyclopropylene Ph CH₂ H (S)- III-609 Me Me Me 1,2-Cyclopropylene Ph CH₂ Me racemic III-610 Me Me Me 1,2-Cyclopropylene Ph CH₂ Me (S)-

TABLE 49

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration III-611 Me Me Me O Ph C(Me)₂CH₂ H racemic III-612 Me Me Me O Ph C(Me)₂CH₂ H (+) III-613 Me Me Me O Ph C(Me)₂CH₂ H (−) III-614 Me Et Me O Ph C(Me)₂CH₂ H racemic III-615 Me Et Me O Ph C(Me)₂CH₂ H (+) III-616 Me Et Me O Ph C(Me)₂CH₂ H (−) III-617 Me Me Me O Ph C(Me)₂CH₂ Me racemic III-618 Me Me Me O Ph C(Me)₂CH₂ Me (+) III-619 Me Me Me O Ph C(Me)₂CH₂ Me (−) III-620 Me Et Me O Ph C(Me)₂CH₂ Me racemic III-621 Me Et Me O Ph C(Me)₂CH₂ Me (+) III-622 Me Et Me O Ph C(Me)₂CH₂ Me (−) III-623 Me Me Me O Ph C(Me)₂CH₂ CHF₂ racemic III-624 Me Me Me O Ph C(Me)₂CH₂ CHF₂ (+) III-625 Me Me Me O Ph C(Me)₂CH₂ CHF₂ (−) III-626 Me Me Me O Ph C(Me)₂CH₂ Et racemic III-627 Me Me Me O Ph C(Me)₂CH₂ Et (+) III-628 Me Me Me O Ph C(Me)₂CH₂ Et (−) III-629 Me Me Me NH Ph C(Me)₂CH₂ H (+) III-630 Me Me Me NH Ph C(Me)₂CH₂ H (−) III-631 Me Et Me NH Ph C(Me)₂CH₂ H (+) III-632 Me Et Me NH Ph C(Me)₂CH₂ H (−) III-633 Me Me Me NH Ph C(Me)₂CH₂ Me racemic III-634 Me Me Me NH Ph C(Me)₂CH₂ Me (+) III-635 Me Me Me NH Ph C(Me)₂CH₂ Me (−) III-636 Me Et Me NH Ph C(Me)₂CH₂ Me racemic III-637 Me Et Me NH Ph C(Me)₂CH₂ Me (+) III-638 Me Et Me NH Ph C(Me)₂CH₂ Me (−) III-639 Me Me Me NH Ph C(Me)₂CH₂ CHF₂ racemic III-640 Me Me Me NH Ph C(Me)₂CH₂ CHF₂ (+) III-641 Me Me Me NH Ph C(Me)₂CH₂ CHF₂ (−) III-642 Me Et Me NH Ph C(Me)₂CH₂ CHF₂ racemic III-643 Me Et Me NH Ph C(Me)₂CH₂ CHF₂ (+) III-644 Me Et Me NH Ph C(Me)₂CH₂ CHF₂ (−) III-645 Me Me Me NH Ph C(Me)₂CH₂ Et racemic III-646 Me Me Me NH Ph C(Me)₂CH₂ Et (+) III-647 Me Me Me NH Ph C(Me)₂CH₂ Et (−) III-648 Me Et Me NH Ph C(Me)₂CH₂ Et racemic III-649 Me Et Me NH Ph C(Me)₂CH₂ Et (+) III-650 Me Et Me NH Ph C(Me)₂CH₂ Et (−)

TABLE 50

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration III-651 Me Me Me NH Ph C(Me)₂CH₂ iPr racemic III-652 Me Me Me NH Ph C(Me)₂CH₂ iPr (+) III-653 Me Me Me NH Ph C(Me)₂CH₂ iPr (−) III-654 Me Et Me NH Ph C(Me)₂CH₂ iPr racemic III-655 Me Et Me NH Ph C(Me)₂CH₂ iPr (+) III-656 Me Et Me NH Ph C(Me)₂CH₂ iPr (−) III-657 Me Me Me NH Ph C(Me)₂CH₂ cPr racemic III-658 Me Me Me NH Ph C(Me)₂CH₂ cPr (+) III-659 Me Me Me NH Ph C(Me)₂CH₂ cPr (−) III-660 Me Et Me NH Ph C(Me)₂CH₂ cPr racemic III-661 Me Et Me NH Ph C(Me)₂CH₂ cPr (+) III-662 Me Et Me NH Ph C(Me)₂CH₂ cPr (−) III-663 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ H racemic III-664 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ H (+) III-665 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ H (−) III-666 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ H racemic III-667 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ H (+) III-668 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ H (−) III-669 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ Me racemic III-670 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ Me (+) III-671 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ Me (−) III-672 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ Me racemic III-673 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ Me (+) III-674 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ Me (−) III-675 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ H racemic III-676 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ H (+) III-677 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ H (−) III-678 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ H racemic III-679 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ H (+) III-680 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ H (−) III-681 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ Me racemic III-682 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ Me (+) III-683 Me Me Me NH Ph 1,1-Cyclopropylene-CH₂ Me (−) III-684 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ Me racemic III-685 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ Me (+) III-686 Me Et Me NH Ph 1,1-Cyclopropylene-CH₂ Me (−) III-687 Me Me Me NH Ph C(Et)₂CH₂ H racemic III-688 Me Me Me NH Ph C(Et)₂CH₂ H (+) III-689 Me Me Me NH Ph C(Et)₂CH₂ H (−) III-690 Me Et Me NH Ph C(Et)₂CH₂ H racemic III-691 Me Et Me NH Ph C(Et)₂CH₂ H (+) III-692 Me Et Me NH Ph C(Et)₂CH₂ H (−) III-693 Me Me Me NH Ph C(Et)₂CH₂ Me racemic III-694 Me Me Me NH Ph C(Et)₂CH₂ Me (+) III-695 Me Me Me NH Ph C(Et)₂CH₂ Me (−) III-696 Me Et Me NH Ph C(Et)₂CH₂ Me racemic III-697 Me Et Me NH Ph C(Et)₂CH₂ Me (+) III-698 Me Et Me NH Ph C(Et)₂CH₂ Me (−) III-699 Me Me Me NH Ph CH₂-1,1-Cyclopropylene H racemic III-700 Me Me Me NH Ph CH₂-1,1-Cyclopropylene H (R)-

TABLE 51 (III)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-701 Me Et Me NH Ph CH₂-1,1-Cyclo- H racemic propylene III-702 Me Et Me NH Ph CH₂-1,1-Cyclo- H (R)- propylene III-703 Me Me Me NH Ph CH₂-1,1-Cyclo- Me racemic propylene III-704 Me Me Me NH Ph CH₂-1,1-Cyclo- Me (R)- propylene III-705 Me Et Me NH Ph CH₂-1,1-Cyclo- Me racemic propylene III-706 Me Et Me NH Ph CH₂-1,1-Cyclo- Me (R)- propylene III-707 Me Me Me NH Ph CH₂-1,1-cyclo- H racemic butylene III-708 Me Me Me NH Ph CH₂-1,1-cyclo- H (R)- butylene III-709 Me Et Me NH Ph CH₂-1,1-cyclo- H racemic butylene III-710 Me Et Me NH Ph CH₂-1,1-cyclo- H (R)- butylene III-711 Me Me Me NH Ph CH₂-1,1-cyclo- Me racemic butylene III-712 Me Me Me NH Ph CH₂-1,1-cyclo- Me (R)- butylene III-713 Me Et Me NH Ph CH₂-1,1-cyclo- Me racemic butylene III-714 Me Et Me NH Ph CH₂-1,1-cyclo- Me (R)- butylene III-715 Me Me Me NH Ph CH₂C(Et)₂ H racemic III-716 Me Me Me NH Ph CH₂C(Et)₂ H (R)- III-717 Me Et Me NH Ph CH₂C(Et)₂ H racemic III-718 Me Et Me NH Ph CH₂C(Et)₂ H (R)- III-719 Me Me Me NH Ph CH₂C(Et)₂ Me racemic III-720 Me Me Me NH Ph CH₂C(Et)₂ Me (R)- III-721 Me Et Me NH Ph CH₂C(Et)₂ Me racemic III-722 Me Et Me NH Ph CH₂C(Et)₂ Me (R)- III-723 Me Me Me NH iPr CH₂ Me racemic III-724 Me Me Me NH iPr CH₂ Me (S)- III-725 Me Et Me NH iPr CH₂ Me racemic III-726 Me Et Me NH iPr CH₂ Me (S)- III-727 Me Me Me NH iPr (CH₂)₂ H racemic III-728 Me Me Me NH iPr (CH₂)₂ H (R)- III-729 Me Et Me NH iPr (CH₂)₂ H racemic III-730 Me Et Me NH iPr (CH₂)₂ H (R)- III-731 Me Me Me NH iPr (CH₂)₂ Me racemic III-732 Me Me Me NH iPr (CH₂)₂ Me (R)- III-733 Me Et Me NH iPr (CH₂)₂ Me racemic III-734 Me Et Me NH iPr (CH₂)₂ Me (R)- III-735 Me Me Me NH CF₃ CH₂ H racemic III-736 Me Me Me NH CF₃ CH₂ H (S)- III-737 Me Et Me NH CF₃ CH₂ H racemic III-738 Me Et Me NH CF₃ CH₂ H (S)- III-739 Me Me Me NH CH₂OH CH₂ H III-740 Me Et Me NH CH₂OH CH₂ H III-741 Me Me Me NH CH₂OMe CH₂ H racemic III-742 Me Me Me NH CH₂OMe CH₂ H (R)- III-743 Me Et Me NH CH₂OMe CH₂ H racemic III-744 Me Et Me NH CH₂OMe CH₂ H (R)- III-745 Me Me Me NH CH₂Ph CH₂ H racemic III-746 Me Me Me NH CH₂Ph CH₂ H (R)- III-747 Me Me Me NH CH₂Ph CH₂ H (S)- III-748 Me Et Me NH CH₂Ph CH₂ H racemic III-749 Me Et Me NH CH₂Ph CH₂ H (S)- III-750 Me Me Me NH 2-F—Ph CH₂ Me racemic

TABLE 52 (III)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-751 Me Me Me NH 2-F—Ph CH₂ Me (S)- III-752 Me Et Me NH 2-F—Ph CH₂ Me racemic III-753 Me Et Me NH 2-F—Ph CH₂ Me (S)- III-754 Me Me Me NH 2-F—Ph (CH₂)₂ H racemic III-755 Me Me Me NH 2-F—Ph (CH₂)₂ H (R)- III-756 Me Et Me NH 2-F—Ph (CH₂)₂ H racemic III-757 Me Et Me NH 2-F—Ph (CH₂)₂ H (R)- III-758 Me Me Me NH 2-F—Ph (CH₂)₂ Me racemic III-759 Me Me Me NH 2-F—Ph (CH₂)₂ Me (R)- III-760 Me Et Me NH 2-F—Ph (CH₂)₂ Me racemic III-761 Me Et Me NH 2-F—Ph (CH₂)₂ Me (R)- III-762 Me Me Me NH 2-F—Ph CH₂C(Me)₂ H racemic III-763 Me Me Me NH 2-F—Ph CH₂C(Me)₂ H (R)- III-764 Me Et Me NH 2-F—Ph CH₂C(Me)₂ H racemic III-765 Me Et Me NH 2-F—Ph CH₂C(Me)₂ H (R)- III-766 Me Me Me NH 2-F—Ph CH₂C(Me)₂ Me racemic III-767 Me Me Me NH 2-F—Ph CH₂C(Me)₂ Me (R)- III-768 Me Et Me NH 2-F—Ph CH₂C(Me)₂ Me racemic III-769 Me Et Me NH 2-F—Ph CH₂C(Me)₂ Me (R)- III-770 Me Me Me NH 2-F—Ph C(Me)₂CH₂ H racemic III-771 Me Me Me NH 2-F—Ph C(Me)₂CH₂ H (+) III-772 Me Me Me NH 2-F—Ph C(Me)₂CH₂ H (−) III-773 Me Et Me NH 2-F—Ph C(Me)₂CH₂ H racemic III-774 Me Et Me NH 2-F—Ph C(Me)₂CH₂ H (+) III-775 Me Et Me NH 2-F—Ph C(Me)₂CH₂ H (−) III-776 Me Me Me NH 2-F—Ph C(Me)₂CH₂ Me racemic III-777 Me Me Me NH 2-F—Ph C(Me)₂CH₂ Me (+) III-778 Me Me Me NH 2-F—Ph C(Me)₂CH₂ Me (−) III-779 Me Et Me NH 2-F—Ph C(Me)₂CH₂ Me racemic III-780 Me Et Me NH 2-F—Ph C(Me)₂CH₂ Me (+) III-781 Me Et Me NH 2-F—Ph C(Me)₂CH₂ Me (−) III-782 Me Me Me NH 2-F—Ph (CH₂)₂ H racemic III-783 Me Me Me NH 2-F—Ph (CH₂)₂ H (R)- III-784 Me Et Me NH 2-F—Ph (CH₂)₂ H racemic III-785 Me Et Me NH 2-F—Ph (CH₂)₂ H (R)- III-786 Me Me Me NH 2-F—Ph (CH₂)₂ Me racemic III-787 Me Me Me NH 2-F—Ph (CH₂)₂ Me (R)- III-788 Me Et Me NH 2-F—Ph (CH₂)₂ Me racemic III-789 Me Et Me NH 2-F—Ph (CH₂)₂ Me (R)- III-790 Me Me Me NH 2-F—Ph CH₂C(Me)₂ H racemic III-791 Me Me Me NH 2-F—Ph CH₂C(Me)₂ H (R)- III-792 Me Et Me NH 2-F—Ph CH₂C(Me)₂ H racemic III-793 Me Et Me NH 2-F—Ph CH₂C(Me)₂ H (R)- III-794 Me Me Me NH 2-F—Ph CH₂C(Me)₂ Me racemic III-795 Me Me Me NH 2-F—Ph CH₂C(Me)₂ Me (R)- III-796 Me Et Me NH 2-F—Ph CH₂C(Me)₂ Me racemic III-797 Me Et Me NH 2-F—Ph CH2C(Me)2 Me (R)- III-798 Me Me Me NH 2-F—Ph C(Me)₂CH₂ H racemic III-799 Me Me Me NH 2-F—Ph C(Me)₂CH₂ H (+) III-800 Me Me Me NH 2-F—Ph C(Me)₂CH₂ H (−)

TABLE 53 (III)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-801 Me Et Me NH 3-F—Ph C(Me)₂CH₂ H racemic III-802 Me Et Me NH 3-F—Ph C(Me)₂CH₂ H (+) III-803 Me Et Me NH 3-F—Ph C(Me)₂CH₂ H (−) III-804 Me Me Me NH 3-F—Ph C(Me)₂CH₂ Me racemic III-805 Me Me Me NH 3-F—Ph C(Me)₂CH₂ Me (+) III-806 Me Me Me NH 3-F—Ph C(Me)₂CH₂ Me (−) III-807 Me Et Me NH 3-F—Ph C(Me)₂CH₂ Me racemic III-808 Me Et Me NH 3-F—Ph C(Me)₂CH₂ Me (+) III-809 Me Et Me NH 3-F—Ph C(Me)₂CH₂ Me (−) III-810 Me Me Me NH 4-F—Ph (CH₂)₂ H racemic III-811 Me Me Me NH 4-F—Ph (CH₂)₂ H (R)- III-812 Me Et Me NH 4-F—Ph (CH₂)₂ H racemic III-813 Me Et Me NH 4-F—Ph (CH₂)₂ H (R)- III-814 Me Me Me NH 4-F—Ph (CH₂)₂ Me racemic III-815 Me Me Me NH 4-F—Ph (CH₂)₂ Me (R)- III-816 Me Et Me NH 4-F—Ph (CH₂)₂ Me racemic III-817 Me Et Me NH 4-F—Ph (CH₂)₂ Me (R)- III-818 Me Me Me NH 4-F—Ph CH₂C(Me)₂ H racemic III-819 Me Me Me NH 4-F—Ph CH₂C(Me)₂ H (R)- III-820 Me Et Me NH 4-F—Ph CH₂C(Me)₂ H racemic III-821 Me Et Me NH 4-F—Ph CH₂C(Me)₂ H (R)- III-822 Me Me Me NH 4-F—Ph CH₂C(Me)₂ Me racemic III-823 Me Me Me NH 4-F—Ph CH₂C(Me)₂ Me (R)- III-824 Me Et Me NH 4-F—Ph CH₂C(Me)₂ Me racemic III-825 Me Et Me NH 4-F—Ph CH₂C(Me)₂ Me (R)- III-826 Me Me Me NH 4-F—Ph C(Me)₂CH₂ H racemic III-827 Me Me Me NH 4-F—Ph C(Me)₂CH₂ H (+) III-828 Me Me Me NH 4-F—Ph C(Me)₂CH₂ H (−) III-829 Me Et Me NH 4-F—Ph C(Me)₂CH₂ H racemic III-830 Me Et Me NH 4-F—Ph C(Me)₂CH₂ H (+) III-831 Me Et Me NH 4-F—Ph C(Me)₂CH₂ H (−) III-832 Me Me Me NH 4-F—Ph C(Me)₂CH₂ Me racemic III-833 Me Me Me NH 4-F—Ph C(Me)₂CH₂ Me (+) III-834 Me Me Me NH 4-F—Ph C(Me)₂CH₂ Me (−) III-835 Me Et Me NH 4-F—Ph C(Me)₂CH₂ Me racemic III-836 Me Et Me NH 4-F—Ph C(Me)₂CH₂ Me (+) III-837 Me Et Me NH 4-F—Ph C(Me)₂CH₂ Me (−) III-838 Me Me Me NH 2-Cl—Ph CH₂ H racemic III-839 Me Me Me NH 2-Cl—Ph CH₂ H (S)- III-840 Me Et Me NH 2-Cl—Ph CH₂ H racemic III-841 Me Et Me NH 2-Cl—Ph CH₂ H (S)- III-842 Me Me Me NH 2-Cl—Ph CH₂ Me racemic III-843 Me Me Me NH 2-Cl—Ph CH₂ Me (S)- III-844 Me Et Me NH 2-Cl—Ph CH₂ Me racemic III-845 Me Et Me NH 2-Cl—Ph CH₂ Me (S)- III-846 Me Me Me NH 2-Cl—Ph (CH₂)₂ H racemic III-847 Me Me Me NH 2-Cl—Ph (CH₂)₂ H (R)- III-848 Me Et Me NH 2-Cl—Ph (CH₂)₂ H racemic III-849 Me Et Me NH 2-Cl—Ph (CH₂)₂ H (R)- III-850 Me Me Me NH 2-Cl—Ph (CH₂)₂ Me racemic

TABLE 54 (IIII)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-851 Me Me Me NH 2-Cl—Ph (CH₂)₂ Me (R)- III-852 Me Et Me NH 2-Cl—Ph (CH₂)₂ Me racemic III-853 Me Et Me NH 2-Cl—Ph (CH₂)₂ Me (R)- III-854 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ H racemic III-855 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ H (R)- III-856 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ H racemic III-857 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ H (R)- III-858 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ Me racemic III-859 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ Me (R)- III-860 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ Me racemic III-861 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ Me (R)- III-862 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ H racemic III-863 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ H (+) III-864 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ H (−) III-865 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ H racemic III-866 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ H (+) III-867 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ H (−) III-868 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ Me racemic III-869 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ Me (+) III-870 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ Me (−) III-871 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ Me racemic III-872 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ Me (+) III-873 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ Me (−) III-874 Me Me Me NH 2-Cl—Ph CH₂ H racemic III-875 Me Me Me NH 2-Cl—Ph CH₂ H (S)- III-876 Me Et Me NH 2-Cl—Ph CH₂ H racemic III-877 Me Et Me NH 2-Cl—Ph CH₂ H (S)- III-878 Me Me Me NH 2-Cl—Ph CH₂ Me racemic III-879 Me Me Me NH 2-Cl—Ph CH₂ Me (S)- III-880 Me Et Me NH 2-Cl—Ph CH₂ Me racemic III-881 Me Et Me NH 2-Cl—Ph CH₂ Me (S)- III-882 Me Me Me NH 2-Cl—Ph (CH₂)₂ H racemic III-883 Me Me Me NH 2-Cl—Ph (CH₂)₂ H (R)- III-884 Me Et Me NH 2-Cl—Ph (CH₂)₂ H racemic III-885 Me Et Me NH 2-Cl—Ph (CH₂)₂ H (R)- III-886 Me Me Me NH 2-Cl—Ph (CH₂)₂ Me racemic III-887 Me Me Me NH 2-Cl—Ph (CH₂)₂ Me (R)- III-888 Me Et Me NH 2-Cl—Ph (CH₂)₂ Me racemic III-889 Me Et Me NH 2-Cl—Ph (CH₂)₂ Me (R)- III-890 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ H racemic III-891 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ H (R)- III-892 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ H racemic III-893 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ H (R)- III-894 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ Me racemic III-895 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ Me (R)- III-896 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ Me racemic III-897 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ Me (R)- III-898 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ H racemic III-899 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ H (+) III-900 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ H (−)

TABLE 55 (III)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-901 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ H racemic III-902 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ H (+) III-903 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ H (−) III-904 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ Me racemic III-905 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ Me (+) III-906 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ Me (−) III-907 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ Me racemic III-908 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ Me (+) III-909 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ Me (−) III-910 Me Me Me NH 3-Cl—Ph CH₂ H racemic III-911 Me Me Me NH 3-Cl—Ph CH₂ H (S)- III-912 Me Et Me NH 3-Cl—Ph CH₂ H racemic III-913 Me Et Me NH 3-Cl—Ph CH₂ H (S)- III-914 Me Me Me NH 3-Cl—Ph CH₂ Me racemic III-915 Me Me Me NH 3-Cl—Ph CH₂ Me (S)- III-916 Me Et Me NH 3-Cl—Ph CH₂ Me racemic III-917 Me Et Me NH 3-Cl—Ph CH₂ Me (S)- III-918 Me Me Me NH 3-Cl—Ph (CH₂)₂ H racemic III-919 Me Me Me NH 3-Cl—Ph (CH₂)₂ H (R)- III-920 Me Et Me NH 3-Cl—Ph (CH₂)₂ H racemic III-921 Me Et Me NH 3-Cl—Ph (CH₂)₂ H (R)- III-922 Me Me Me NH 3-Cl—Ph (CH₂)₂ Me racemic III-923 Me Me Me NH 3-Cl—Ph (CH₂)₂ Me (R)- III-924 Me Et Me NH 3-Cl—Ph (CH₂)₂ Me racemic III-925 Me Et Me NH 3-Cl—Ph (CH₂)₂ Me (R)- III-926 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ H racemic III-927 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ H (R)- III-928 Me Et Me NH 3-Cl—Ph CH₂C(Me)₂ H racemic III-929 Me Et Me NH 3-Cl—Ph CH₂C(Me)₂ H (R)- III-930 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ Me racemic III-931 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ Me (R)- III-932 Me Et Me NH 3-Cl—Ph CH₂C(Me)₂ Me racemic III-933 Me Et Me NH 3-Cl—Ph CH₂C(Me)₂ Me (R)- III-934 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ H racemic III-935 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ H (+) III-936 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ H (−) III-937 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ H racemic III-938 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ H (+) III-939 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ H (−) III-940 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ Me racemic III-941 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ Me (+) III-942 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ Me (−) III-943 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ Me racemic III-944 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ Me (+) III-945 Me Et Me NH 4-Cl—Ph C(Me)₂CH₂ Me (−) III-946 Me Me Me NH 2-Me—Ph CH₂ H racemic III-947 Me Me Me NH 2-Me—Ph CH₂ H (S)- III-948 Me Et Me NH 2-Me—Ph CH₂ H racemic III-949 Me Et Me NH 2-Me—Ph CH₂ H (S)- III-950 Me Me Me NH 2-Me—Ph CH₂ Me racemic

TABLE 56 (III)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-951 Me Me Me NH 2-Me—Ph CH₂ Me (S)- III-952 Me Et Me NH 2-Me—Ph CH₂ Me racemic III-953 Me Et Me NH 2-Me—Ph CH₂ Me (S)- III-954 Me Me Me NH 2-Me—Ph (CH₂)₂ H racemic III-955 Me Me Me NH 2-Me—Ph (CH₂)₂ H (R)- III-956 Me Et Me NH 2-Me—Ph (CH₂)₂ H racemic III-957 Me Et Me NH 2-Me—Ph (CH₂)₂ H (R)- III-958 Me Me Me NH 2-Me—Ph (CH₂)₂ Me racemic III-959 Me Me Me NH 2-Me—Ph (CH₂)₂ Me (R)- III-960 Me Et Me NH 2-Me—Ph (CH₂)₂ Me racemic III-961 Me Et Me NH 2-Me—Ph (CH₂)₂ Me (R)- III-962 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ H racemic III-963 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ H (R)- III-964 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ H racemic III-965 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ H (R)- III-966 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ Me racemic III-967 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ Me (R)- III-968 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ Me racemic III-969 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ Me (R)- III-970 Me Me Me NH 2-Me—Ph C(Me)₂CH₂ H racemic III-971 Me Me Me NH 2-Me—Ph C(Me)₂CH₂ H (+) III-972 Me Me Me NH 2-Me—Ph C(Me)₂CH₂ H (−) III-973 Me Et Me NH 2-Me—Ph C(Me)₂CH₂ H racemic III-974 Me Et Me NH 2-Me—Ph C(Me)₂CH₂ H (+) III-975 Me Et Me NH 2-Me—Ph C(Me)₂CH₂ H (−) III-976 Me Me Me NH 2-Me—Ph C(Me)₂CH₂ Me racemic III-977 Me Me Me NH 2-Me—Ph C(Me)₂CH₂ Me (+) III-978 Me Me Me NH 2-Me—Ph C(Me)₂CH₂ Me (−) III-979 Me Et Me NH 2-Me—Ph C(Me)₂CH₂ Me racemic III-980 Me Et Me NH 2-Me—Ph C(Me)₂CH₂ Me (+) III-981 Me Et Me NH 2-Me—Ph C(Me)₂CH₂ Me (−) III-982 Me Me Me NH 3-Me—Ph CH₂ H racemic III-983 Me Me Me NH 3-Me—Ph CH₂ H (S)- III-984 Me Et Me NH 3-Me—Ph CH₂ H racemic III-985 Me Et Me NH 3-Me—Ph CH₂ H (S)- III-986 Me Me Me NH 3-Me—Ph CH₂ Me racemic III-987 Me Me Me NH 3-Me—Ph CH₂ Me (S)- III-988 Me Et Me NH 3-Me—Ph CH₂ Me racemic III-989 Me Et Me NH 3-Me—Ph CH₂ Me (S)- III-990 Me Me Me NH 3-Me—Ph (CH₂)₂ H racemic III-991 Me Me Me NH 3-Me—Ph (CH₂)₂ H (R)- III-992 Me Et Me NH 3-Me—Ph (CH₂)₂ H racemic III-993 Me Et Me NH 3-Me—Ph (CH₂)₂ H (R)- III-994 Me Me Me NH 3-Me—Ph (CH₂)₂ Me racemic III-995 Me Me Me NH 3-Me—Ph (CH₂)₂ Me (R)- III-996 Me Et Me NH 3-Me—Ph (CH₂)₂ Me racemic III-997 Me Et Me NH 3-Me—Ph (CH₂)₂ Me (R)- III-998 Me Me Me NH 3-Me—Ph CH₂C(Me)₂ H racemic III-999 Me Me Me NH 3-Me—Ph CH₂C(Me)₂ H (R)- III-1000 Me Et Me NH 3-Me—Ph CH₂C(Me)₂ H racemic

TABLE 57 (III)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-1001 Me Et Me NH 3-Me—Ph CH₂C(Me)₂ H (R)- III-1002 Me Me Me NH 3-Me—Ph CH₂C(Me)₂ Me racemic III-1003 Me Me Me NH 3-Me—Ph CH₂C(Me)₂ Me (R)- III-1004 Me Et Me NH 3-Me—Ph CH₂C(Me)₂ Me racemic III-1005 Me Et Me NH 3-Me—Ph CH₂C(Me)₂ Me (R)- III-1006 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ H racemic III-1007 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ H (+) III-1008 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ H (−) III-1009 Me Et Me NH 3-Me—Ph C(Me)₂CH₂ H racemic III-1010 Me Et Me NH 3-Me—Ph C(Me)₂CH₂ H (+) III-1011 Me Et Me NH 3-Me—Ph C(Me)₂CH₂ H (−) III-1012 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ Me racemic III-1013 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ Me (+) III-1014 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ Me (−) III-1015 Me Et Me NH 3-Me—Ph C(Me)₂CH₂ Me racemic III-1016 Me Et Me NH 3-Me—Ph C(Me)₂CH₂ Me (+) III-1017 Me Et Me NH 3-Me—Ph C(Me)₂CH₂ Me (−) III-1018 Me Me Me NH 4-Me—Ph CH₂ H racemic III-1019 Me Me Me NH 4-Me—Ph CH₂ H (S)- III-1020 Me Et Me NH 4-Me—Ph CH₂ H racemic III-1021 Me Et Me NH 4-Me—Ph CH₂ H (S)- III-1022 Me Me Me NH 4-Me—Ph CH₂ Me racemic III-1023 Me Me Me NH 4-Me—Ph CH₂ Me (S)- III-1024 Me Et Me NH 4-Me—Ph CH₂ Me racemic III-1025 Me Et Me NH 4-Me—Ph CH₂ Me (S)- III-1026 Me Me Me NH 4-Me—Ph (CH₂)₂ H racemic III-1027 Me Me Me NH 4-Me—Ph (CH₂)₂ H (R)- III-1028 Me Et Me NH 4-Me—Ph (CH₂)₂ H racemic III-1029 Me Et Me NH 4-Me—Ph (CH₂)₂ H (R)- III-1030 Me Me Me NH 4-Me—Ph (CH₂)₂ Me racemic III-1031 Me Me Me NH 4-Me—Ph (CH₂)₂ Me (R)- III-1032 Me Et Me NH 4-Me—Ph (CH₂)₂ Me racemic III-1033 Me Et Me NH 4-Me—Ph (CH₂)₂ Me (R)- III-1034 Me Me Me NH 4-Me—Ph CH₂C(Me)₂ H racemic III-1035 Me Me Me NH 4-Me—Ph CH₂C(Me)₂ H (R)- III-1036 Me Et Me NH 4-Me—Ph CH₂C(Me)₂ H racemic III-1037 Me Et Me NH 4-Me—Ph CH₂C(Me)₂ H (R)- III-1038 Me Me Me NH 4-Me—Ph CH₂C(Me)₂ Me racemic III-1039 Me Me Me NH 4-Me—Ph CH₂C(Me)₂ Me (R)- III-1040 Me Et Me NH 4-Me—Ph CH₂C(Me)₂ Me racemic III-1041 Me Et Me NH 4-Me—Ph CH₂C(Me)₂ Me (R)- III-1042 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ H racemic III-1043 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ H (+) III-1044 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ H (−) III-1045 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ H racemic III-1046 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ H (+) III-1047 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ H (−) III-1048 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ Me racemic III-1049 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ Me (+) III-1050 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ Me (−)

TABLE 58 (III)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-1051 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ Me racemic III-1052 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ Me (+) III-1053 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ Me (−) III-1054 Me Me Me — Ph — H racemic III-1055 Me Me Me — Ph — H (R)- III-1056 Me Et Me — Ph — H racemic III-1057 Me Et Me — Ph — H (R)- III-1058 Me Me Me — Ph — Me racemic III-1059 Me Me Me — Ph — Me (R)- III-1060 Me Et Me — Ph — Me racemic III-1061 Me Et Me — Ph — Me (R)- III-1062 Me Me Me — Ph — CHF₂ racemic III-1063 Me Me Me — Ph — CHF₂ (R)- III-1064 Me Et Me — Ph — CHF₂ racemic III-1065 Me Et Me — Ph — CHF₂ (R)- III-1066 Me Me Me — Ph — CF₃ racemic III-1067 Me Me Me — Ph — CF₃ (R)- III-1068 Me Et Me — Ph — CF₃ racemic III-1069 Me Et Me — Ph — CF₃ (R)- III-1070 Me Me Me — Ph — Et racemic III-1071 Me Me Me — Ph — Et (R)- III-1072 Me Et Me — Ph — Et racemic III-1073 Me Et Me — Ph — Et (R)- III-1074 Me Me Me — Ph — CF₂CH₃ Cracemic III-1075 Me Me Me — Ph — CF₂CH₃ (R)- III-1076 Me Et Me — Ph — CF₂CH₃ Cracemic III-1077 Me Et Me — Ph — CF₂CH₃ (R)- III-1078 Me Me Me — Ph — nPr racemic III-1079 Me Me Me — Ph — nPr (R)- III-1080 Me Et Me — Ph — nPr racemic III-1081 Me Et Me — Ph — nPr (R)- III-1082 Me Me Me — Ph — nBu racemic III-1083 Me Me Me — Ph — nBu (R)- III-1084 Me Et Me — Ph — nBu racemic III-1085 Me Et Me — Ph — nBu (R)- III-1086 Me Me Me — Ph — iPr racemic III-1087 Me Me Me — Ph — iPr (R)- III-1088 Me Et Me — Ph — iPr racemic III-1089 Me Et Me — Ph — iPr (R)- III-1090 Me Me Me — Ph — cPr racemic III-1091 Me Me Me — Ph — cPr (R)- III-1092 Me Et Me — Ph — cPr racemic III-1093 Me Et Me — Ph — cPr (R)- III-1094 Me Me Me — Ph — Ph racemic III-1095 Me Me Me — Ph — Ph (R)- III-1096 Me Et Me — Ph — Ph racemic III-1097 Me Et Me — Ph — Ph (R)- III-1098 Me Me Me — Ph CH₂ CHF₂ racemic III-1099 Me Me Me — Ph CH₂ CHF₂ (S)- III-1100 Me Me Me — Ph CH₂ Et racemic

TABLE 59 (III)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-1101 Me Me Me — Ph CH₂ Et (S)- III-1102 Me Me Me — Ph CH₂ Ph racemic III-1103 Me Me Me — Ph CH₂ Ph (R)- III-1104 Me Me Me — Ph (CH₂)₂ H racemic III-1105 Me Me Me — Ph (CH₂)₂ H (S)- III-1106 Me Me Me — Ph (CH₂)₂ Me racemic III-1107 Me Me Me — Ph (CH₂)₂ Me (S)- III-1108 Me Me Me — Ph (CH₂)₂ CHF₂ racemic III-1109 Me Me Me — Ph (CH₂)₂ CHF₂ (S)- III-1110 Me Me Me — Ph (CH₂)₂ Et racemic III-1111 Me Me Me — Ph (CH₂)₂ Et (S)- III-1112 Me Me Me — H — H III-1113 Me Me Me — H — Me III-1114 Me Me Me — H — CHF₂ III-1115 Me Me Me — H — CF₃ III-1116 Me Me Me — H — Et III-1117 Me Me Me — H — nPr III-1118 Me Me Me — H — iPr III-1119 Me Me Me — H — cPr III-1120 Me Me Me — H — Ph III-1121 Me Me Me — Me — H racemic III-1122 Me Me Me — Me — H (R)- III-1123 Me Me Me — Me — Me racemic III-1124 Me Me Me — Me — Me (R)- III-1125 Me Me Me — Me — CHF₂ racemic III-1126 Me Me Me — Me — CHF₂ (R)- III-1127 Me Me Me — Me — CF₃ racemic III-1128 Me Me Me — Me — CF₃ (R)- III-1129 Me Me Me — Me — Et racemic III-1130 Me Me Me — Me — Et (R)- III-1131 Me Me Me — Me — nPr racemic III-1132 Me Me Me — Me — nPr (R)- III-1133 Me Me Me — Me — iPr racemic III-1134 Me Me Me — Me — iPr (R)- III-1135 Me Me Me — Me — cPr racemic III-1136 Me Me Me — Me — cPr (R)- III-1137 Me Me Me — Me — cHex racemic III-1138 Me Me Me — Me — cHex (R)- III-1139 Me Me Me — Me — Ph racemic III-1140 Me Me Me — Me — Ph (R)- III-1141 Me Me Me — Me — 2-F—Ph racemic III-1142 Me Me Me — Me — 2-F—Ph (R)- III-1143 Me Me Me — Me — 3-F—Ph racemic III-1144 Me Me Me — Me — 3-F—Ph (R)- III-1145 Me Me Me — Me — 4-F—Ph racemic III-1146 Me Me Me — Me — 4-F—Ph (R)- III-1147 Me Me Me — Me — 2-Cl—Ph racemic III-1148 Me Me Me — Me — 2-Cl—Ph (R)- III-1149 Me Me Me — Me — 3-Cl—Ph racemic III-1150 Me Me Me — Me — 3-Cl—Ph (R)-

TABLE 60 (III)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-1151 Me Me Me — Me — 4-Cl—Ph racemic III-1152 Me Me Me — Me — 4-Cl—Ph (R)- III-1153 Me Me Me — Me — 2-Py racemic III-1154 Me Me Me — Me — 2-Py (R)- III-1155 Me Me Me — Me — 3-Py racemic III-1156 Me Me Me — Me — 3-Py (R)- III-1157 Me Me Me — Me — 4-Py racemic III-1158 Me Me Me — Me — 4-Py (R)- III-1159 Me Me Me — iPr — H racemic III-1160 Me Me Me — iPr — H (R)- III-1161 Me Me Me — iPr — Me racemic III-1162 Me Me Me — iPr — Me (R)- III-1163 Me Me Me — iPr — CHF₂ racemic III-1164 Me Me Me — iPr — CHF₂ (R)- III-1165 Me Me Me — iPr — CF₃ racemic III-1166 Me Me Me — iPr — CF₃ (R)- III-1167 Me Me Me — iPr — Et racemic III-1168 Me Me Me — iPr — Et (R)- III-1169 Me Me Me — iPr — nPr racemic III-1170 Me Me Me — iPr — nPr (R)- III-1171 Me Me Me — iPr — iPr racemic III-1172 Me Me Me — iPr — iPr (R)- III-1173 Me Me Me — iPr — cPr racemic III-1174 Me Me Me — iPr — cPr (R)- III-1175 Me Me Me — iPr — Ph racemic III-1176 Me Me Me — iPr — Ph (R)- III-1177 Me Me Me — CF₃ — H racemic III-1178 Me Me Me — CF₃ — H (R)- III-1179 Me Me Me — CF₃ — Me racemic III-1180 Me Me Me — CF₃ — Me (R)- III-1181 Me Me Me — CF₃ — CHF₂ racemic III-1182 Me Me Me — CF₃ — CHF₂ (R)- III-1183 Me Me Me — CF₃ — CF₃ racemic III-1184 Me Me Me — CF₃ — CF₃ (R)- III-1185 Me Me Me — CF₃ — Et racemic III-1186 Me Me Me — CF₃ — Et (R)- III-1187 Me Me Me — CF₃ — nPr racemic III-1188 Me Me Me — CF₃ — nPr (R)- III-1189 Me Me Me — CF₃ — iPr racemic III-1190 Me Me Me — CF₃ — iPr (R)- III-1191 Me Me Me — CF₃ — cPr racemic III-1192 Me Me Me — CF₃ — cPr (R)- III-1193 Me Me Me — CF₃ — Ph racemic III-1194 Me Me Me — CF₃ — Ph (R)- III-1195 Me Me Me — CH₂OH — H racemic III-1196 Me Me Me — CH₂OH — H (R)- III-1197 Me Me Me — CH₂OH — Me racemic III-1198 Me Me Me — CH₂OH — Me (R)- III-1199 Me Me Me — CH₂OH — CHF₂ racemic III-1200 Me Me Me — CH₂OH — CHF₂ (R)-

TABLE 61 (III)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-1201 Me Me Me — CH₂OH — CF₃ racemic III-1202 Me Me Me — CH₂OH — CF₃ (R)- III-1203 Me Me Me — CH₂OH — Et racemic III-1204 Me Me Me — CH₂OH — Et (R)- III-1205 Me Me Me — CH₂OH — nPr racemic III-1206 Me Me Me — CH₂OH — nPr (R)- III-1207 Me Me Me — CH₂OH — iPr racemic III-1208 Me Me Me — CH₂OH — iPr (R)- III-1209 Me Me Me — CH₂OH — cPr racemic III-1210 Me Me Me — CH₂OH — cPr (R)- III-1211 Me Me Me — CH₂OH — Ph racemic III-1212 Me Me Me — CH₂OH — Ph (R)- III-1213 Me Me Me — CH₂OMe — H racemic III-1214 Me Me Me — CH₂OMe — H (R)- III-1215 Me Me Me — CH₂OMe — Me racemic III-1216 Me Me Me — CH₂OMe — Me (R)- III-1217 Me Me Me — CH₂OMe — CHF₂ racemic III-1218 Me Me Me — CH₂OMe — CHF₂ (R)- III-1219 Me Me Me — CH₂OMe — CF₃ racemic III-1220 Me Me Me — CH₂OMe — CF₃ (R)- III-1221 Me Me Me — CH₂OMe — Et racemic III-1222 Me Me Me — CH₂OMe — Et (R)- III-1223 Me Me Me — CH₂OMe — nPr racemic III-1224 Me Me Me — CH₂OMe — nPr (R)- III-1225 Me Me Me — CH₂OMe — iPr racemic III-1226 Me Me Me — CH₂OMe — iPr (R)- III-1227 Me Me Me — CH₂OMe — cPr racemic III-1228 Me Me Me — CH₂OMe — cPr (R)- III-1229 Me Me Me — CH₂OMe — Ph racemic III-1230 Me Me Me — CH₂OMe — Ph (R)- III-1231 Me Me Me — CH₂OBn — H racemic III-1232 Me Me Me — CH₂OBn — H (R)- III-1233 Me Me Me — CH₂OBn — Me racemic III-1234 Me Me Me — CH₂OBn — Me (R)- III-1235 Me Me Me — CH₂OBn — Ph racemic III-1236 Me Me Me — CH₂OBn — Ph (R)- III-1237 Me Me Me — CH₂NMe₂ — H racemic III-1238 Me Me Me — CH₂NMe₂ — H (R)- III-1239 Me Me Me — CH₂NMe₂ — Me racemic III-1240 Me Me Me — CH₂NMe₂ — Me (R)- III-1241 Me Me Me — CH₂NMe₂ — CHF₂ racemic III-1242 Me Me Me — CH₂NMe₂ — CHF₂ (R)- III-1243 Me Me Me — CH₂NMe₂ — CF₃ racemic III-1244 Me Me Me — CH₂NMe₂ — CF₃ (R)- III-1245 Me Me Me — CH₂NMe₂ — Et racemic III-1246 Me Me Me — CH₂NMe₂ — Et (R)- III-1247 Me Me Me — CH₂NMe₂ — nPr racemic III-1248 Me Me Me — CH₂NMe₂ — nPr (R)- III-1249 Me Me Me — CH₂NMe₂ — iPr racemic III-1250 Me Me Me — CH₂NMe₂ — iPr (R)-

TABLE 62 (III)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁵ uration III-1251 Me Me Me — CH₂NMe₂ — cPr racemic III-1252 Me Me Me — CH₂NMe₂ — cPr (R)- III-1253 Me Me Me — CH₂NMe₂ — Ph racemic III-1254 Me Me Me — CH₂NMe₂ — Ph (R)- III-1255 Me Me Me — CH₂-(3,3-difluoro — H racemic — pyrrolidyl) — III-1256 Me Me Me — CH₂-(3,3-difluoro — H (R)- — pyrrolidyl) — III-1257 Me Me Me — CH₂-(3,3-difluoro — Me racemic — pyrrolidyl) — III-1258 Me Me Me — CH₂-(3,3-difluoro — Me (R)- — pyrrolidyl) — III-1259 Me Me Me — CH₂-(3,3-difluoro — Ph racemic — pyrrolidyl) — III-1260 Me Me Me — CH₂-(3,3-difluoro — Ph (R)- — pyrrolidyl) — III-1261 Me Me Me — 2-F—Ph — H racemic III-1262 Me Me Me — 2-F—Ph — H (R)- III-1263 Me Me Me — 2-F—Ph — Me racemic III-1264 Me Me Me — 2-F—Ph — Me (R)- III-1265 Me Me Me — 2-F—Ph — CHF₂ racemic III-1266 Me Me Me — 2-F—Ph — CHF₂ (R)- III-1267 Me Me Me — 2-F—Ph — CF₃ racemic III-1268 Me Me Me — 2-F—Ph — CF₃ (R)- III-1269 Me Me Me — 2-F—Ph — Et racemic III-1270 Me Me Me — 2-F—Ph — Et (R)- III-1271 Me Me Me — 2-F—Ph — nPr racemic III-1272 Me Me Me — 2-F—Ph — nPr (R)- III-1273 Me Me Me — 2-F—Ph — iPr racemic III-1274 Me Me Me — 2-F—Ph — iPr (R)- III-1275 Me Me Me — 2-F—Ph — cPr racemic III-1276 Me Me Me — 2-F—Ph — cPr (R)- III-1277 Me Me Me — 2-F—Ph — H racemic III-1278 Me Me Me — 2-F—Ph — H (R)- III-1279 Me Me Me — 2-F—Ph — Me racemic III-1280 Me Me Me — 2-F—Ph — Me (R)- III-1281 Me Me Me — 2-F—Ph — CHF₂ racemic III-1282 Me Me Me — 2-F—Ph — CHF₂ (R)- III-1283 Me Me Me — 2-F—Ph — CF₃ racemic III-1284 Me Me Me — 2-F—Ph — CF₃ (R)- III-1285 Me Me Me — 2-F—Ph — Et racemic III-1286 Me Me Me — 2-F—Ph — Et (R)- III-1287 Me Me Me — 2-F—Ph — nPr racemic III-1288 Me Me Me — 2-F—Ph — nPr (R)- III-1289 Me Me Me — 2-F—Ph — iPr racemic III-1290 Me Me Me — 2-F—Ph — iPr (R)- III-1291 Me Me Me — 2-F—Ph — cPr racemic III-1292 Me Me Me — 2-F—Ph — cPr (R)- III-1293 Me Me Me — 2-F—Ph — H racemic III-1294 Me Me Me — 2-F—Ph — H (R)- III-1295 Me Me Me — 2-F—Ph — Me racemic III-1296 Me Me Me — 2-F—Ph — Me (R)- III-1297 Me Me Me — 2-F—Ph — CHF₂ racemic III-1298 Me Me Me — 2-F—Ph — CHF₂ (R)- III-1299 Me Me Me — 2-F—Ph — CF₃ racemic III-1300 Me Me Me — 2-F—Ph — CF₃ (R)-

TABLE 63 (III)

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration III-1301 Me Me Me — 4-F—Ph — Et racemic III-1302 Me Me Me — 4-F—Ph — Et (R)- III-1303 Me Me Me — 4-F—Ph — nPr racemic III-1304 Me Me Me — 4-F—Ph — nPr (R)- III-1305 Me Me Me — 4-F—Ph — iPr racemic III-1306 Me Me Me — 4-F—Ph — iPr (R)- III-1307 Me Me Me — 4-F—Ph — cPr racemic III-1308 Me Me Me — 4-F—Ph — cPr (R)- III-1309 Me Me Me — 2-thienyl — H racemic III-1310 Me Me Me — 2-thienyl — H (S)- III-1311 Me Me Me — 2-thienyl — Me racemic III-1312 Me Me Me — 2-thienyl — Me (S)- III-1313 Me Me Me — 2-thienyl — CHF₂ racemic III-1314 Me Me Me — 2-thienyl — CHF₂ (S)- III-1315 Me Me Me — 2-thienyl — CF₃ racemic III-1316 Me Me Me — 2-thienyl — CF₃ (S)- III-1317 Me Me Me — 2-thienyl — Et racemic III-1318 Me Me Me — 2-thienyl — Et (S)- III-1319 Me Me Me — 2-thienyl — nPr racemic III-1320 Me Me Me — 2-thienyl — nPr (S)- III-1321 Me Me Me — 2-thienyl — iPr racemic III-1322 Me Me Me — 2-thienyl — iPr (S)- III-1323 Me Me Me — 2-thienyl — cPr racemic III-1324 Me Me Me — 2-thienyl — cPr (S)- III-1325 Me Me Me — 3-thienyl — H racemic III-1326 Me Me Me — 3-thienyl — H (R)- III-1327 Me Me Me — 3-thienyl — Me racemic III-1328 Me Me Me — 3-thienyl — Me (R)- III-1329 Me Me Me — 3-thienyl — CHF₂ racemic III-1330 Me Me Me — 3-thienyl — CHF₂ (R)- III-1331 Me Me Me — 3-thienyl — CF₃ racemic III-1332 Me Me Me — 3-thienyl — CF₃ (R)- III-1333 Me Me Me — 3-thienyl — Et racemic III-1334 Me Me Me — 3-thienyl — Et (R)- III-1335 Me Me Me — 3-thienyl — nPr racemic III-1336 Me Me Me — 3-thienyl — nPr (R)- III-1337 Me Me Me — 3-thienyl — iPr racemic III-1338 Me Me Me — 3-thienyl — iPr (R)- III-1339 Me Me Me — 3-thienyl — cPr racemic III-1340 Me Me Me — 3-thienyl — cPr (R)-

TABLE 64 (IV)

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration IV-1  Me Me Me O Ph CH₂ H racemic IV-2  Me Me Me O Ph CH₂ H (S)- IV-3  Me Et Me O Ph CH₂ H racemic IV-4  Me Et Me O Ph CH₂ H (S)- IV-5  Me Me Me O Ph CH₂ Me racemic IV-6  Me Me Me O Ph CH₂ Me (S)- IV-7  Me Et Me O Ph CH₂ Me racemic IV-8  Me Et Me O Ph CH₂ Me (S)- IV-9  Me Me Me O Ph CH₂ CHF₂ racemic IV-10 Me Me Me O Ph CH₂ CHF₂ (S)- IV-11 Me Et Me O Ph CH₂ CHF₂ racemic IV-12 Me Et Me O Ph CH₂ CHF₂ (S)- IV-13 Me Me Me O Ph CH₂ Et racemic IV-14 Me Me Me O Ph CH₂ Et (S)- IV-15 Me Et Me O Ph CH₂ Et racemic IV-16 Me Et Me O Ph CH₂ Et (S)- IV-17 Me Me Me O Ph CH₂ iPr racemic IV-18 Me Me Me O Ph CH₂ iPr (S)- IV-19 Me Et Me O Ph CH₂ iPr racemic IV-20 Me Et Me O Ph CH₂ iPr (S)- IV-21 Me Me Me O Ph CH₂ cPr racemic IV-22 Me Me Me O Ph CH₂ cPr (S)- IV-23 Me Et Me O Ph CH₂ cPr racemic IV-24 Me Et Me O Ph CH₂ cPr (S)- IV-25 Me Me Me O Ph CH₂ Ph racemic IV-26 Me Me Me O Ph CH₂ Ph (S)- IV-27 Me Et Me O Ph CH₂ Ph racemic IV-28 Me Et Me O Ph CH₂ Ph (S)- IV-29 Me Me Me O Ph C(Me)₂ H racemic IV-30 Me Me Me O Ph C(Me)₂ H (S)- IV-31 Me Et Me O Ph C(Me)₂ H racemic IV-32 Me Et Me O Ph C(Me)₂ H (S)- IV-33 Me Me Me O Ph C(Me)₂ Me racemic IV-34 Me Me Me O Ph C(Me)₂ Me (S)- IV-35 Me Et Me O Ph C(Me)₂ Me racemic IV-36 Me Et Me O Ph C(Me)₂ Me (S)- IV-37 Me Me Me O Ph C(Me)₂ CHF₂ racemic IV-38 Me Me Me O Ph C(Me)₂ CHF₂ (S)- IV-39 Me Et Me O Ph C(Me)₂ CHF₂ racemic IV-40 Me Et Me O Ph C(Me)₂ CHF₂ (S)- IV-41 Me Me Me O Ph C(Me)₂ Et racemic IV-42 Me Me Me O Ph C(Me)₂ Et (S)- IV-43 Me Et Me O Ph C(Me)₂ Et racemic IV-44 Me Et Me O Ph C(Me)₂ Et (S)- IV-45 Me Me Me O Ph C(Me)₂ iPr racemic IV-46 Me Me Me O Ph C(Me)₂ iPr (S)- IV-47 Me Et Me O Ph C(Me)₂ iPr racemic IV-48 Me Et Me O Ph C(Me)₂ iPr (S)- IV-49 Me Me Me O Ph C(Me)₂ cPr racemic IV-50 Me Me Me O Ph C(Me)₂ cPr (S)-

TABLE 65 (IV)

Com- pound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration IV-51 Me Et Me O Ph C(Me)₂ cPr racemic IV-52 Me Et Me O Ph C(Me)₂ cPr (S)- IV-53 Me Me Me O Ph C(Me)₂ Ph racemic IV-54 Me Me Me O Ph C(Me)₂ Ph (S)- IV-55 Me Et Me O Ph C(Me)₂ Ph racemic IV-56 Me Et Me O Ph C(Me)₂ Ph (S)- IV-57 Me Me Me O Ph (CH₂)₂ H racemic IV-58 Me Me Me O Ph (CH₂)₂ H (R)- IV-59 Me Et Me O Ph (CH₂)₂ H racemic IV-60 Me Et Me O Ph (CH₂)₂ H (R)- IV-61 Me Me Me O Ph (CH₂)₂ Me racemic IV-62 Me Me Me O Ph (CH₂)₂ Me (R)- IV-63 Me Et Me O Ph (CH₂)₂ Me racemic IV-64 Me Et Me O Ph (CH₂)₂ Me (R)- IV-65 Me Me Me O Ph (CH₂)₂ CHF₂ racemic IV-66 Me Me Me O Ph (CH₂)₂ CHF₂ (R)- IV-67 Me Et Me O Ph (CH₂)₂ CHF₂ racemic IV-68 Me Et Me O Ph (CH₂)₂ CHF₂ (R)- IV-69 Me Me Me O Ph (CH₂)₂ Et racemic IV-70 Me Me Me O Ph (CH₂)₂ Et (R)- IV-71 Me Et Me O Ph (CH₂)₂ Et racemic IV-72 Me Et Me O Ph (CH₂)₂ Et (R)- IV-73 Me Me Me O Ph (CH₂)₂ iPr racemic IV-74 Me Me Me O Ph (CH₂)₂ iPr (R)- IV-75 Me Et Me O Ph (CH₂)₂ iPr racemic IV-76 Me Et Me O Ph (CH₂)₂ iPr (R)- IV-77 Me Me Me O Ph (CH₂)₂ cPr racemic IV-78 Me Me Me O Ph (CH₂)₂ cPr (R)- IV-79 Me Et Me O Ph (CH₂)₂ cPr racemic IV-80 Me Et Me O Ph (CH₂)₂ cPr (R)- IV-81 Me Me Me O Ph (CH₂)₂ Ph racemic IV-82 Me Me Me O Ph (CH₂)₂ Ph (R)- IV-83 Me Et Me O Ph (CH₂)₂ Ph racemic IV-84 Me Et Me O Ph (CH₂)₂ Ph (R)- IV-85 Me Me Me O Ph CH₂C(Me)₂ H racemic IV-86 Me Me Me O Ph CH₂C(Me)₂ H (R)- IV-87 Me Et Me O Ph CH₂C(Me)₂ H racemic IV-88 Me Et Me O Ph CH₂C(Me)₂ H (R)- IV-89 Me Me Me O Ph CH₂C(Me)₂ Me racemic IV-90 Me Me Me O Ph CH₂C(Me)₂ Me (R)- IV-91 Me Et Me O Ph CH₂C(Me)₂ Me racemic IV-92 Me Et Me O Ph CH₂C(Me)₂ Me (R)- IV-93 Me Me Me O Ph CH₂C(Me)₂ CHF₂ racemic IV-94 Me Me Me O Ph CH₂C(Me)₂ CHF₂ (R)- IV-95 Me Et Me O Ph CH₂C(Me)₂ CHF₂ racemic IV-96 Me Et Me O Ph CH₂C(Me)₂ CHF₂ (R)- IV-97 Me Me Me O Ph CH₂C(Me)₂ Et racemic IV-98 Me Me Me O Ph CH₂C(Me)₂ Et (R)- IV-99 Me Et Me O Ph CH₂C(Me)₂ Et racemic  IV-100 Me Et Me O Ph CH₂C(Me)₂ Et (R)-

TABLE 66 (IV)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration IV-101 Me Me Me O Ph CH₂C(Me)₂ iPr racemic IV-102 Me Me Me O Ph CH₂C(Me)₂ iPr (R)- IV-103 Me Et Me O Ph CH₂C(Me)₂ iPr racemic IV-104 Me Et Me O Ph CH₂C(Me)₂ iPr (R)- IV-105 Me Me Me O Ph CH₂C(Me)₂ cPr racemic IV-106 Me Me Me O Ph CH₂C(Me)₂ cPr (R)- IV-107 Me Et Me O Ph CH₂C(Me)₂ cPr racemic IV-108 Me Et Me O Ph CH₂C(Me)₂ cPr (R)- IV-109 Me Me Me O Ph CH₂C(Me)₂ Ph racemic IV-110 Me Me Me O Ph CH₂C(Me)₂ Ph (R)- IV-111 Me Et Me O Ph CH₂C(Me)₂ Ph racemic IV-112 Me Et Me O Ph CH₂C(Me)₂ Ph (R)- IV-113 Me Me Me NH Ph CH₂ H racemic IV-114 Me Me Me NH Ph CH₂ H (S)- IV-115 Me Me Me NH Ph CH₂ H (R)- IV-116 Me Et Me NH Ph CH₂ H racemic IV-117 Me Et Me NH Ph CH₂ H (S)- IV-118 Me Me Me N(Me) Ph CH₂ H racemic IV-119 Me Me Me N(Me) Ph CH₂ H (S)- IV-120 Me Et Me N(Me) Ph CH₂ H racemic IV-121 Me Et Me N(Me) Ph CH₂ H (S)- IV-122 Me Me Me NH Ph CH₂ Me racemic IV-123 Me Me Me NH Ph CH₂ Me (S)- IV-124 Me Et Me NH Ph CH₂ Me racemic IV-125 Me Et Me NH Ph CH₂ Me (S)- IV-126 Me Me Me N(Me) Ph CH₂ Me racemic IV-127 Me Me Me N(Me) Ph CH₂ Me (S)- IV-128 Me Et Me N(Me) Ph CH₂ Me racemic IV-129 Me Et Me N(Me) Ph CH₂ Me (S)- IV-130 Me Me Me NH Ph CH₂ CHF₂ racemic IV-131 Me Me Me NH Ph CH₂ CHF₂ (S)- IV-132 Me Et Me NH Ph CH₂ CHF₂ racemic IV-133 Me Et Me NH Ph CH₂ CHF₂ (S)- IV-134 Me Me Me N(Me) Ph CH₂ CHF₂ racemic IV-135 Me Me Me N(Me) Ph CH₂ CHF₂ (S)- IV-136 Me Et Me N(Me) Ph CH₂ CHF₂ racemic IV-137 Me Et Me N(Me) Ph CH₂ CHF₂ (S)- IV-138 Me Me Me NH Ph CH₂ Et racemic IV-139 Me Me Me NH Ph CH₂ Et (S)- IV-140 Me Et Me NH Ph CH₂ Et racemic IV-141 Me Et Me NH Ph CH₂ Et (S)- IV-142 Me Me Me N(Me) Ph CH₂ Et racemic IV-143 Me Me Me N(Me) Ph CH₂ Et (S)- IV-144 Me Et Me N(Me) Ph CH₂ Et racemic IV-145 Me Et Me N(Me) Ph CH₂ Et (S)- IV-146 Me Me Me NH Ph CH₂ iPr racemic IV-147 Me Me Me NH Ph CH₂ iPr (S)- IV-148 Me Et Me NH Ph CH₂ iPr racemic IV-149 Me Et Me NH Ph CH₂ iPr (S)- IV-150 Me Me Me N(Me) Ph CH₂ iPr racemic

TABLE 67 (IV)

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration IV-151 Me Me Me N(Me) Ph CH₂ iPr (S)- IV-152 Me Et Me N(Me) Ph CH₂ iPr racemic IV-153 Me Et Me N(Me) Ph CH₂ iPr (S)- IV-154 Me Me Me NH Ph CH₂ cPr racemic IV-155 Me Me Me NH Ph CH₂ cPr (S)- IV-156 Me Et Me NH Ph CH₂ cPr racemic IV-157 Me Et Me NH Ph CH₂ cPr (S)- IV-158 Me Me Me N(Me) Ph CH₂ cPr racemic IV-159 Me Me Me N(Me) Ph CH₂ cPr (S)- IV-160 Me Et Me N(Me) Ph CH₂ cPr racemic IV-161 Me Et Me N(Me) Ph CH₂ cPr (S)- IV-162 Me Me Me NH Ph CH₂ Ph racemic IV-163 Me Me Me NH Ph CH₂ Ph (S)- IV-164 Me Et Me NH Ph CH₂ Ph racemic IV-165 Me Et Me NH Ph CH₂ Ph (S)- IV-166 Me Me Me N(Me) Ph CH₂ Ph racemic IV-167 Me Me Me N(Me) Ph CH₂ Ph (S)- IV-168 Me Et Me N(Me) Ph CH₂ Ph racemic IV-169 Me Et Me N(Me) Ph CH₂ Ph (S)- IV-170 Me Me Me NH Ph C(Me)₂ H racemic IV-171 Me Me Me NH Ph C(Me)₂ H (S)- IV-172 Me Et Me NH Ph C(Me)₂ H racemic IV-173 Me Et Me NH Ph C(Me)₂ H (S)- IV-174 Me Me Me N(Me) Ph C(Me)₂ H racemic IV-175 Me Me Me N(Me) Ph C(Me)₂ H (S)- IV-176 Me Et Me N(Me) Ph C(Me)₂ H racemic IV-177 Me Et Me N(Me) Ph C(Me)₂ H (S)- IV-178 Me Me Me NH Ph C(Me)₂ Me racemic IV-179 Me Me Me NH Ph C(Me)₂ Me (S)- IV-180 Me Et Me NH Ph C(Me)₂ Me racemic IV-181 Me Et Me NH Ph C(Me)₂ Me (S)- IV-182 Me Me Me N(Me) Ph C(Me)₂ Me racemic IV-183 Me Me Me N(Me) Ph C(Me)₂ Me (S)- IV-184 Me Et Me N(Me) Ph C(Me)₂ Me racemic IV-185 Me Et Me N(Me) Ph C(Me)₂ Me (S)- IV-186 Me Me Me NH Ph C(Me)₂ CHF₂ racemic IV-187 Me Me Me NH Ph C(Me)₂ CHF₂ (S)- IV-188 Me Et Me NH Ph C(Me)₂ CHF₂ racemic IV-189 Me Et Me NH Ph C(Me)₂ CHF₂ (S)- IV-190 Me Me Me N(Me) Ph C(Me)₂ CHF₂ racemic IV-191 Me Me Me N(Me) Ph C(Me)₂ CHF₂ (S)- IV-192 Me Et Me N(Me) Ph C(Me)₂ CHF₂ racemic IV-193 Me Et Me N(Me) Ph C(Me)₂ CHF₂ (S)- IV-194 Me Me Me NH Ph C(Me)₂ Et racemic IV-195 Me Me Me NH Ph C(Me)₂ Et (S)- IV-196 Me Et Me NH Ph C(Me)₂ Et racemic IV-197 Me Et Me NH Ph C(Me)₂ Et (S)- IV-198 Me Me Me N(Me) Ph C(Me)₂ Et racemic IV-199 Me Me Me N(Me) Ph C(Me)₂ Et (S)- IV-200 Me Et Me N(Me) Ph C(Me)₂ Et racemic

TABLE 68 (IV)

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration IV-201 Me Et Me N(Me) Ph C(Me)₂ Et (S)- IV-202 Me Me Me NH Ph C(Me)₂ iPr racemic IV-203 Me Me Me NH Ph C(Me)₂ iPr (S)- IV-204 Me Et Me NH Ph C(Me)₂ iPr racemic IV-205 Me Et Me NH Ph C(Me)₂ iPr (S)- IV-206 Me Me Me N(Me) Ph C(Me)₂ iPr racemic IV-207 Me Me Me N(Me) Ph C(Me)₂ iPr (S)- IV-208 Me Et Me N(Me) Ph C(Me)₂ iPr racemic IV-209 Me Et Me N(Me) Ph C(Me)₂ iPr (S)- IV-210 Me Me Me NH Ph C(Me)₂ cPr racemic IV-211 Me Me Me NH Ph C(Me)₂ cPr (S)- IV-212 Me Et Me NH Ph C(Me)₂ cPr racemic IV-213 Me Et Me NH Ph C(Me)₂ cPr (S)- IV-214 Me Me Me N(Me) Ph C(Me)₂ cPr racemic IV-215 Me Me Me N(Me) Ph C(Me)₂ cPr (S)- IV-216 Me Et Me N(Me) Ph C(Me)₂ cPr racemic IV-217 Me Et Me N(Me) Ph C(Me)₂ cPr (S)- IV-218 Me Me Me NH Ph C(Me)₂ Ph racemic IV-219 Me Me Me NH Ph C(Me)₂ Ph (S)- IV-220 Me Et Me NH Ph C(Me)₂ Ph racemic IV-221 Me Et Me NH Ph C(Me)₂ Ph (S)- IV-222 Me Me Me N(Me) Ph C(Me)₂ Ph racemic IV-223 Me Me Me N(Me) Ph C(Me)₂ Ph (S)- IV-224 Me Et Me N(Me) Ph C(Me)₂ Ph racemic IV-225 Me Et Me N(Me) Ph C(Me)₂ Ph (S)- IV-226 Me Me Me NH Ph (CH₂)₂ H racemic IV-227 Me Me Me NH Ph (CH₂)₂ H (R)- IV-228 Me Et Me NH Ph (CH₂)₂ H racemic IV-229 Me Et Me NH Ph (CH₂)₂ H (R)- IV-230 Me Me Me N(Me) Ph (CH₂)₂ H racemic IV-231 Me Me Me N(Me) Ph (CH₂)₂ H (R)- IV-232 Me Et Me N(Me) Ph (CH₂)₂ H racemic IV-233 Me Et Me N(Me) Ph (CH₂)₂ H (R)- IV-234 Me Me Me NH Ph (CH₂)₂ Me racemic IV-235 Me Me Me NH Ph (CH₂)₂ Me (R)- IV-236 Me Et Me NH Ph (CH₂)₂ Me racemic IV-237 Me Et Me NH Ph (CH₂)₂ Me (R)- IV-238 Me Me Me N(Me) Ph (CH₂)₂ Me racemic IV-239 Me Me Me N(Me) Ph (CH₂)₂ Me (R)- IV-240 Me Et Me N(Me) Ph (CH₂)₂ Me racemic IV-241 Me Et Me N(Me) Ph (CH₂)₂ Me (R)- IV-242 Me Me Me NH Ph (CH₂)₂ CHF₂ racemic IV-243 Me Me Me NH Ph (CH₂)₂ CHF₂ (R)- IV-244 Me Et Me NH Ph (CH₂)₂ CHF₂ racemic IV-245 Me Et Me NH Ph (CH₂)₂ CHF₂ (R)- IV-246 Me Me Me N(Me) Ph (CH₂)₂ CHF₂ racemic IV-247 Me Me Me N(Me) Ph (CH₂)₂ CHF₂ (R)- IV-248 Me Et Me N(Me) Ph (CH₂)₂ CHF₂ racemic IV-249 Me Et Me N(Me) Ph (CH₂)₂ CHF₂ (R)- IV-250 Me Me Me NH Ph (CH₂)₂ Et racemic

TABLE 69 (IV)

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration IV-251 Me Me Me NH Ph (CH₂)₂ Et (R)- IV-252 Me Et Me NH Ph (CH₂)₂ Et racemic IV-253 Me Et Me NH Ph (CH₂)₂ Et (R)- IV-254 Me Me Me N(Me) Ph (CH₂)₂ Et racemic IV-255 Me Me Me N(Me) Ph (CH₂)₂ Et (R)- IV-256 Me Et Me N(Me) Ph (CH₂)₂ Et racemic IV-257 Me Et Me N(Me) Ph (CH₂)₂ Et (R)- IV-258 Me Me Me NH Ph (CH₂)₂ iPr racemic IV-259 Me Me Me NH Ph (CH₂)₂ iPr (R)- IV-260 Me Et Me NH Ph (CH₂)₂ iPr racemic IV-261 Me Et Me NH Ph (CH₂)₂ iPr (R)- IV-262 Me Me Me N(Me) Ph (CH₂)₂ iPr racemic IV-263 Me Me Me N(Me) Ph (CH₂)₂ iPr (R)- IV-264 Me Et Me N(Me) Ph (CH₂)₂ iPr racemic IV-265 Me Et Me N(Me) Ph (CH₂)₂ iPr (R)- IV-266 Me Me Me NH Ph (CH₂)₂ cPr racemic IV-267 Me Me Me NH Ph (CH₂)₂ cPr (R)- IV-268 Me Et Me NH Ph (CH₂)₂ cPr racemic IV-269 Me Et Me NH Ph (CH₂)₂ cPr (R)- IV-270 Me Me Me N(Me) Ph (CH₂)₂ cPr racemic IV-271 Me Me Me N(Me) Ph (CH₂)₂ cPr (R)- IV-272 Me Et Me N(Me) Ph (CH₂)₂ cPr racemic IV-273 Me Et Me N(Me) Ph (CH₂)₂ cPr (R)- IV-274 Me Me Me NH Ph (CH₂)₂ Ph racemic IV-275 Me Me Me NH Ph (CH₂)₂ Ph (R)- IV-276 Me Et Me NH Ph (CH₂)₂ Ph racemic IV-277 Me Et Me NH Ph (CH₂)₂ Ph (R)- IV-278 Me Me Me N(Me) Ph (CH₂)₂ Ph racemic IV-279 Me Me Me N(Me) Ph (CH₂)₂ Ph (R)- IV-280 Me Et Me N(Me) Ph (CH₂)₂ Ph racemic IV-281 Me Et Me N(Me) Ph (CH₂)₂ Ph (R)- IV-282 Me Me Me NH Ph (CH₂)₃ H racemic IV-283 Me Me Me NH Ph (CH₂)₃ H (R)- IV-284 Me Et Me NH Ph (CH₂)₃ H racemic IV-285 Me Et Me NH Ph (CH₂)₃ H (R)- IV-286 Me Me Me N(Me) Ph (CH₂)₃ H racemic IV-287 Me Me Me N(Me) Ph (CH₂)₃ H (R)- IV-288 Me Et Me N(Me) Ph (CH₂)₃ H racemic IV-289 Me Et Me N(Me) Ph (CH₂)₃ H (R)- IV-290 Me Me Me NH Ph (CH₂)₄ H racemic IV-291 Me Me Me NH Ph (CH₂)₄ H (R)- IV-292 Me Et Me NH Ph (CH₂)₄ H racemic IV-293 Me Et Me NH Ph (CH₂)₄ H (R)- IV-294 Me Me Me N(Me) Ph (CH₂)₄ H racemic IV-295 Me Me Me N(Me) Ph (CH₂)₄ H (R)- IV-296 Me Et Me N(Me) Ph (CH₂)₄ H racemic IV-297 Me Et Me N(Me) Ph (CH₂)₄ H (R)- IV-298 Me Me Me NH Ph CH₂C(Me)₂ H racemic IV-299 Me Me Me NH Ph CH₂C(Me)₂ H (R)- IV-300 Me Et Me NH Ph CH₂C(Me)₂ H racemic

TABLE 70 (IV)

Com- pound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration IV-301 Me Et Me NH Ph CH₂C(Me)₂ H (R)- IV-302 Me Me Me N(Me) Ph CH₂C(Me)₂ H racemic IV-303 Me Me Me N(Me) Ph CH₂C(Me)₂ H (R)- IV-304 Me Et Me N(Me) Ph CH₂C(Me)₂ H racemic IV-305 Me Et Me N(Me) Ph CH₂C(Me)₂ H (R)- IV-306 Me Me Me NH Ph CH₂C(Me)₂ Me racemic IV-307 Me Me Me NH Ph CH₂C(Me)₂ Me (R)- IV-308 Me Et Me NH Ph CH₂C(Me)₂ Me racemic IV-309 Me Et Me NH Ph CH₂C(Me)₂ Me (R)- IV-310 Me Me Me N(Me) Ph CH₂C(Me)₂ Me racemic IV-311 Me Me Me N(Me) Ph CH₂C(Me)₂ Me (R)- IV-312 Me Et Me N(Me) Ph CH₂C(Me)₂ Me racemic IV-313 Me Et Me N(Me) Ph CH₂C(Me)₂ Me (R)- IV-314 Me Me Me NH Ph CH₂C(Me)₂ CHF₂ racemic IV-315 Me Me Me NH Ph CH₂C(Me)₂ CHF₂ (R)- IV-316 Me Et Me NH Ph CH₂C(Me)₂ CHF₂ racemic IV-317 Me Et Me NH Ph CH₂C(Me)₂ CHF₂ (R)- IV-318 Me Me Me N(Me) Ph CH₂C(Me)₂ CHF₂ racemic IV-319 Me Me Me N(Me) Ph CH₂C(Me)₂ CHF₂ (R)- IV-320 Me Et Me N(Me) Ph CH₂C(Me)₂ CHF₂ racemic IV-321 Me Et Me N(Me) Ph CH₂C(Me)₂ CHF₂ (R)- IV-322 Me Me Me NH Ph CH₂C(Me)₂ Et racemic IV-323 Me Me Me NH Ph CH₂C(Me)₂ Et (R)- IV-324 Me Et Me NH Ph CH₂C(Me)₂ Et racemic IV-325 Me Et Me NH Ph CH₂C(Me)₂ Et (R)- IV-326 Me Me Me N(Me) Ph CH₂C(Me)₂ Et racemic IV-327 Me Me Me N(Me) Ph CH₂C(Me)₂ Et (R)- IV-328 Me Et Me N(Me) Ph CH₂C(Me)₂ Et racemic IV-329 Me Et Me N(Me) Ph CH₂C(Me)₂ Et (R)- IV-330 Me Me Me NH Ph CH₂C(Me)₂ iPr racemic IV-331 Me Me Me NH Ph CH₂C(Me)₂ iPr (R)- IV-332 Me Et Me NH Ph CH₂C(Me)₂ iPr racemic IV-333 Me Et Me NH Ph CH₂C(Me)₂ iPr (R)- IV-334 Me Me Me N(Me) Ph CH₂C(Me)₂ iPr racemic IV-335 Me Me Me N(Me) Ph CH₂C(Me)₂ iPr (R)- IV-336 Me Et Me N(Me) Ph CH₂C(Me)₂ iPr racemic IV-337 Me Et Me N(Me) Ph CH₂C(Me)₂ iPr (R)- IV-338 Me Me Me NH Ph CH₂C(Me)₂ cPr racemic IV-339 Me Me Me NH Ph CH₂C(Me)₂ cPr (R)- IV-340 Me Et Me NH Ph CH₂C(Me)₂ cPr racemic IV-341 Me Et Me NH Ph CH₂C(Me)₂ cPr (R)- IV-342 Me Me Me N(Me) Ph CH₂C(Me)₂ cPr racemic IV-343 Me Me Me N(Me) Ph CH₂C(Me)₂ cPr (R)- IV-344 Me Et Me N(Me) Ph CH₂C(Me)₂ cPr racemic IV-345 Me Et Me N(Me) Ph CH₂C(Me)₂ cPr (R)- IV-346 Me Me Me NH Ph CH₂C(Me)₂ Ph racemic IV-347 Me Me Me NH Ph CH₂C(Me)₂ Ph (R)- IV-348 Me Et Me NH Ph CH₂C(Me)₂ Ph racemic IV-349 Me Et Me NH Ph CH₂C(Me)₂ Ph (R)- IV-350 Me Me Me N(Me) Ph CH₂C(Me)₂ Ph racemic

TABLE 71 (IV)

Com- Con- pound figu- No. R¹ R² R³ L² R⁴ L³ R⁵ ration IV-351 Me Me Me N(Me) Ph CH₂C(Me)₂ Ph (R)- IV-352 Me Et Me N(Me) Ph CH₂C(Me)₂ Ph racemic IV-353 Me Et Me N(Me) Ph CH₂C(Me)₂ Ph (R)- IV-354 Me Me Me NH Ph C(Me)₂CH₂ H racemic IV-355 Me Me Me NH Ph C(Me)₂CH₂ H (S)- IV-356 Me Et Me NH Ph C(Me)₂CH₂ H racemic IV-357 Me Et Me NH Ph C(Me)₂CH₂ H (S)- IV-358 Me Me Me N(Me) Ph C(Me)₂CH₂ H racemic IV-359 Me Me Me N(Me) Ph C(Me)₂CH₂ H (S)- IV-360 Me Et Me N(Me) Ph C(Me)₂CH₂ H racemic IV-361 Me Et Me N(Me) Ph C(Me)₂CH₂ H (S)- IV-362 Me Me Me NH Ph CF₂CH₂ H racemic IV-363 Me Me Me NH Ph CF₂CH₂ H (S)- IV-364 Me Et Me NH Ph CF₂CH₂ H racemic IV-365 Me Et Me NH Ph CF₂CH₂ H (S)- IV-366 Me Me Me N(Me) Ph CF₂CH₂ H racemic IV-367 Me Me Me N(Me) Ph CF₂CH₂ H (S)- IV-368 Me Et Me N(Me) Ph CF₂CH₂ H racemic IV-369 Me Et Me N(Me) Ph CF₂CH₂ H (S)- IV-370 Me Me Me NH Ph CH═CHCH₂ H racemic IV-371 Me Me Me NH Ph CH═CHCH₂ H (S)- IV-372 Me Et Me NH Ph CH═CHCH₂ H racemic IV-373 Me Et Me NH Ph CH═CHCH₂ H (S)- IV-374 Me Me Me N(Me) Ph CH═CHCH₂ H racemic IV-375 Me Me Me N(Me) Ph CH═CHCH₂ H (S)- IV-376 Me Et Me N(Me) Ph CH═CHCH₂ H racemic IV-377 Me Et Me N(Me) Ph CH═CHCH₂ H (S)- IV-378 Me Me Me NH Ph C≡CCH₂ H racemic IV-379 Me Me Me NH Ph C≡CCH₂ H (S)- IV-380 Me Et Me NH Ph C≡CCH₂ H racemic IV-381 Me Et Me NH Ph C≡CCH₂ H (S)- IV-382 Me Me Me N(Me) Ph C≡CCH₂ H racemic IV-383 Me Me Me N(Me) Ph C≡CCH₂ H (S)- IV-384 Me Et Me N(Me) Ph C≡CCH₂ H racemic IV-385 Me Et Me N(Me) Ph C≡CCH₂ H (S)- IV-386 Me Me Me NH Ph 1,1-Cyclopropylene H racemic IV-387 Me Me Me NH Ph 1,1-Cyclopropylene H (S)- IV-388 Me Et Me NH Ph 1,1-Cyclopropylene H racemic IV-389 Me Et Me NH Ph 1,1-Cyclopropylene H (S)- IV-390 Me Me Me N(Me) Ph 1,1-Cyclopropylene H racemic IV-391 Me Me Me N(Me) Ph 1,1-Cyclopropylene H (S)- IV-392 Me Et Me N(Me) Ph 1,1-Cyclopropylene H racemic IV-393 Me Et Me N(Me) Ph 1,1-Cyclopropylene H (S)- IV-394 Me Me Me NH Ph 1,2-Cyclo- H racemic propynylene IV-395 Me Me Me NH Ph 1,2-Cyclo- H (S)- propynylene IV-396 Me Et Me NH Ph 1,2-Cyclo- H racemic propynylene IV-397 Me Et Me NH Ph 1,2-Cyclo- H (S)- propynylene IV-398 Me Me Me N(Me) Ph 1,2-Cyclo- H racemic propynylene IV-399 Me Me Me N(Me) Ph 1,2-Cyclo- H (S)- propynylene IV-400 Me Et Me N(Me) Ph 1,2-Cyclo- H racemic propynylene

TABLE 72 (IV)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration IV-401 Me Et Me N(Me) Ph 1,2-Cyclo- H (S)- propynylene IV-402 Me Me Me NH Ph C(═O) H racemic IV-403 Me Me Me NH Ph C(═O) H (S)- IV-404 Me Et Me NH Ph C(═O) H racemic IV-405 Me Et Me NH Ph C(═O) H (S)- IV-406 Me Me Me N(Me) Ph C(═O) H racemic IV-407 Me Me Me N(Me) Ph C(═O) H (S)- IV-408 Me Et Me N(Me) Ph C(═O) H racemic IV-409 Me Et Me N(Me) Ph C(═O) H (S)- IV-410 Me Me Me NH Ph C(═O) Bn racemic IV-411 Me Me Me NH Ph C(═O) Bn (S)- IV-412 Me Et Me NH Ph C(═O) Bn racemic IV-413 Me Et Me NH Ph C(═O) Bn (S)- IV-414 Me Me Me N(Me) Ph C(═O) Bn racemic IV-415 Me Me Me N(Me) Ph C(═O) Bn (S)- IV-416 Me Et Me N(Me) Ph C(═O) Bn racemic IV-417 Me Et Me N(Me) Ph C(═O) Bn (S)- IV-418 Me Me Me NH Ph C(═O) Me racemic IV-419 Me Me Me NH Ph C(═O) Me (S)- IV-420 Me Et Me NH Ph C(═O) Me racemic IV-421 Me Et Me NH Ph C(═O) Me (S)- IV-422 Me Me Me N(Me) Ph C(═O) Me racemic IV-423 Me Me Me N(Me) Ph C(═O) Me (S)- IV-424 Me Et Me N(Me) Ph C(═O) Me racemic IV-425 Me Et Me N(Me) Ph C(═O) Me (S)- IV-426 Me Me Me NH Ph CH(Me) H racemic IV-427 Me Me Me NH Ph CH(Me) H (S)- IV-428 Me Et Me NH Ph CH(Me) H racemic IV-429 Me Et Me NH Ph CH(Me) H (S)- IV-430 Me Me Me NH Ph CH(iPr) H racemic IV-431 Me Me Me NH Ph CH(iPr) H (S)- IV-432 Me Et Me NH Ph CH(iPr) H racemic IV-433 Me Et Me NH Ph CH(iPr) H (S)- IV-434 Me Me Me NH Ph CH(Ph) H racemic IV-435 Me Me Me NH Ph CH(Ph) H (S)- IV-436 Me Et Me NH Ph CH(Ph) H racemic IV-437 Me Et Me NH Ph CH(Ph) H (S)- IV-438 Me Me Me NH H CH₂ H IV-439 Me Et Me NH H CH₂ H IV-440 Me Me Me N(Me) H CH₂ H IV-441 Me Et Me N(Me) H CH₂ H IV-442 Me Me Me NH H CH(Me) H IV-443 Me Et Me NH H CH(Me) H IV-444 Me Me Me N(Me) H CH(Me) H IV-445 Me Et Me N(Me) H CH(Me) H IV-446 Me Me Me NH H CH(iPr) H IV-447 Me Et Me NH H CH(iPr) H IV-448 Me Me Me N(Me) H CH(iPr) H IV-449 Me Et Me N(Me) H CH(iPr) H IV-450 Me Me Me NH H CH(Ph) H

TABLE 73 (IV)

Compound No. R¹ R² R³ L² R⁴ L³ R⁵ Configuration IV-451 Me Et Me NH H CH(Ph) H IV-452 Me Me Me N(Me) H CH(Ph) H IV-453 Me Et Me N(Me) H CH(Ph) H IV-454 Me Me Me NH Me CH₂ H racemic IV-455 Me Me Me NH Me CH₂ H (S)- IV-456 Me Et Me NH Me CH₂ H racemic IV-457 Me Et Me NH Me CH₂ H (S)- IV-458 Me Me Me NH Me CH(Me) H racemic IV-459 Me Me Me NH Me CH(Me) H (S)- IV-460 Me Et Me NH Me CH(Me) H racemic IV-461 Me Et Me NH Me CH(Me) H (S)- IV-462 Me Me Me NH Me CH(iPr) H racemic IV-463 Me Me Me NH Me CH(iPr) H (S)- IV-464 Me Et Me NH Me CH(iPr) H racemic IV-465 Me Et Me NH Me CH(iPr) H (S)- IV-466 Me Me Me NH Me CH(Ph) H racemic IV-467 Me Me Me NH Me CH(Ph) H (S)- IV-468 Me Et Me NH Me CH(Ph) H racemic IV-469 Me Et Me NH Me CH(Ph) H (S)- IV-470 Me Me Me N(Me) Me CH₂ H racemic IV-471 Me Me Me N(Me) Me CH₂ H (S)- IV-472 Me Et Me N(Me) Me CH₂ H racemic IV-473 Me Et Me N(Me) Me CH₂ H (S)- IV-474 Me Me Me NH iPr CH₂ H racemic IV-475 Me Me Me NH iPr CH₂ H (S)- IV-476 Me Et Me NH iPr CH₂ H racemic IV-477 Me Et Me NH iPr CH₂ H (S)- IV-478 Me Me Me NH iPr CH(Me) H racemic IV-479 Me Me Me NH iPr CH(Me) H (S)- IV-480 Me Et Me NH iPr CH(Me) H racemic IV-481 Me Et Me NH iPr CH(Me) H (S)- IV-482 Me Me Me NH iPr CH(iPr) H racemic IV-483 Me Me Me NH iPr CH(iPr) H (S)- IV-484 Me Et Me NH iPr CH(iPr) H racemic IV-485 Me Et Me NH iPr CH(iPr) H (S)- IV-486 Me Me Me NH iPr CH(Ph) H racemic IV-487 Me Me Me NH iPr CH(Ph) H (S)- IV-488 Me Et Me NH iPr CH(Ph) H racemic IV-489 Me Et Me NH iPr CH(Ph) H (S)- IV-490 Me Me Me N(Me) iPr CH₂ H racemic IV-491 Me Me Me N(Me) iPr CH₂ H (S)- IV-492 Me Et Me N(Me) iPr CH₂ H racemic IV-493 Me Et Me N(Me) iPr CH₂ H (S)- IV-494 Me Me Me NH cHex CH₂ H racemic IV-495 Me Me Me NH cHex CH₂ H (S)- IV-496 Me Et Me NH cHex CH₂ H racemic IV-497 Me Et Me NH cHex CH₂ H (S)- IV-498 Me Me Me N(Me) cHex CH₂ H racemic IV-499 Me Me Me N(Me) cHex CH₂ H (S)- IV-500 Me Et Me N(Me) cHex CH₂ H racemic

TABLE 74 (IV)

Com- pound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration IV-501 Me Et Me N(Me) cHex CH₂ H (S)- IV-502 Me Me Me NH 1,3-Benzo- CH₂ H racemic dioxol-4-yl IV-503 Me Me Me NH 1,3-Benzo- CH₂ H (S)- dioxol-4-yl IV-504 Me Et Me NH 1,3-Benzo- CH₂ H racemic dioxol-4-yl IV-505 Me Et Me NH 1,3-Benzo- CH₂ H (S)- dioxol-4-yl IV-506 Me Me Me N(Me) 1,3-Benzo- CH₂ H racemic dioxol-4-yl IV-507 Me Me Me N(Me) 1,3-Benzo- CH₂ H (S)- dioxol-4-yl IV-508 Me Et Me N(Me) 1,3-Benzo- CH₂ H racemic dioxol-4-yl IV-509 Me Et Me N(Me) 1,3-Benzo- CH₂ H (S)- dioxol-4-yl IV-510 Me Me Me NH 2-F—Ph CH₂ H racemic IV-511 Me Me Me NH 2-F—Ph CH₂ H (S)- IV-512 Me Et Me NH 2-F—Ph CH₂ H racemic IV-513 Me Et Me NH 2-F—Ph CH₂ H (S)- IV-514 Me Me Me N(Me) 2-F—Ph CH₂ H racemic IV-515 Me Me Me N(Me) 2-F—Ph CH₂ H (S)- IV-516 Me Et Me N(Me) 2-F—Ph CH₂ H racemic IV-517 Me Et Me N(Me) 2-F—Ph CH₂ H (S)- IV-518 Me Me Me NH 3-F—Ph CH₂ H racemic IV-519 Me Me Me NH 3-F—Ph CH₂ H (S)- IV-520 Me Et Me NH 3-F—Ph CH₂ H racemic IV-521 Me Et Me NH 3-F—Ph CH₂ H (S)- IV-522 Me Me Me N(Me) 3-F—Ph CH₂ H racemic IV-523 Me Me Me N(Me) 3-F—Ph CH₂ H (S)- IV-524 Me Et Me N(Me) 3-F—Ph CH₂ H racemic IV-525 Me Et Me N(Me) 3-F—Ph CH₂ H (S)- IV-526 Me Me Me NH 4-F—Ph CH₂ H racemic IV-527 Me Me Me NH 4-F—Ph CH₂ H (S)- IV-528 Me Et Me NH 4-F—Ph CH₂ H racemic IV-529 Me Et Me NH 4-F—Ph CH₂ H (S)- IV-530 Me Me Me N(Me) 4-F—Ph CH₂ H racemic IV-531 Me Me Me N(Me) 4-F—Ph CH₂ H (S)- IV-532 Me Et Me N(Me) 4-F—Ph CH₂ H racemic IV-533 Me Et Me N(Me) 4-F—Ph CH₂ H (S)- IV-534 Me Me Me NH 2-Py CH₂ H racemic IV-535 Me Me Me NH 2-Py CH₂ H (S)- IV-536 Me Et Me NH 2-Py CH₂ H racemic IV-537 Me Et Me NH 2-Py CH₂ H (S)- IV-538 Me Me Me N(Me) 2-Py CH₂ H racemic IV-539 Me Me Me N(Me) 2-Py CH₂ H (S)- IV-540 Me Et Me N(Me) 2-Py CH₂ H racemic IV-541 Me Et Me N(Me) 2-Py CH₂ H (S)- IV-542 Me Me Me NH 3-Py CH₂ H racemic IV-543 Me Me Me NH 3-Py CH₂ H (S)- IV-544 Me Et Me NH 3-Py CH₂ H racemic IV-545 Me Et Me NH 3-Py CH₂ H (S)- IV-546 Me Me Me N(Me) 3-Py CH₂ H racemic IV-547 Me Me Me N(Me) 3-Py CH₂ H (S)- IV-548 Me Et Me N(Me) 3-Py CH₂ H racemic IV-549 Me Et Me N(Me) 3-Py CH₂ H (S)- IV-550 Me Me Me NH 4-Py CH₂ H racemic

TABLE 75 (IV)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁵ tion IV-551 Me Me Me NH 4-Py CH₂ H (S)- IV-552 Me Et Me NH 4-Py CH₂ H racemic IV-553 Me Et Me NH 4-Py CH₂ H (S)- IV-554 Me Me Me N(Me) 4-Py CH₂ H racemic IV-555 Me Me Me N(Me) 4-Py CH₂ H (S)- IV-556 Me Et Me N(Me) 4-Py CH₂ H racemic IV-557 Me Et Me N(Me) 4-Py CH₂ H (S)- IV-558 Me Me Me CH₂ Ph CH₂ H racemic IV-559 Me Me Me CH₂ Ph CH₂ H (S)- IV-560 Me Et Me CH₂ Ph CH₂ H racemic IV-561 Me Et Me CH₂ Ph CH₂ H (S)- IV-562 Me Me Me CH₂ Ph — H racemic IV-563 Me Me Me CH₂ Ph — H (S)- IV-564 Me Et Me CH₂ Ph — H racemic IV-565 Me Et Me CH₂ Ph — H (S)- IV-566 Me Me Me CH₂ Ph CH₂ Me racemic IV-567 Me Me Me CH₂ Ph CH₂ Me (S)- IV-568 Me Et Me CH₂ Ph CH₂ Me racemic IV-569 Me Et Me CH₂ Ph CH₂ Me (S)- IV-570 Me Me Me CH₂ Ph CH₂ CHF₂ racemic IV-571 Me Me Me CH₂ Ph CH₂ CHF₂ (S)- IV-572 Me Me Me CH₂ Ph CH₂ Et racemic IV-573 Me Me Me CH₂ Ph CH₂ Et (S)- IV-574 Me Et Me CH₂ Ph CH₂ Et racemic IV-575 Me Et Me CH₂ Ph CH₂ Et (S)- IV-576 Me Me Me CH₂ Ph CH₂ cPr racemic IV-577 Me Me Me CH₂ Ph CH₂ cPr (S)- IV-578 Me Et Me CH₂ Ph CH₂ cPr racemic IV-579 Me Et Me CH₂ Ph CH₂ cPr (S)- IV-580 Me Me Me CH₂ Ph CH₂ Ph racemic IV-581 Me Me Me CH₂ Ph CH₂ Ph (S)- IV-582 Me Et Me CH₂ Ph CH₂ Ph racemic IV-583 Me Et Me CH₂ Ph CH₂ Ph (S)- IV-584 Me Me Me CH₂ Ph C(Me)₂ H racemic IV-585 Me Me Me CH₂ Ph C(Me)₂ H (S)- IV-586 Me Et Me CH₂ Ph C(Me)₂ H racemic IV-587 Me Et Me CH₂ Ph C(Me)₂ H (S)- IV-588 Me Me Me CH₂ Ph C(Me)₂ Me racemic IV-589 Me Me Me CH₂ Ph C(Me)₂ Me (S)- IV-590 Me Et Me CH₂ Ph C(Me)₂ Me racemic IV-591 Me Et Me CH₂ Ph C(Me)₂ Me (S)- IV-592 Me Me Me CH₂ Ph C(Me)₂ CHF₂ racemic IV-593 Me Me Me CH₂ Ph C(Me)₂ CHF₂ (S)- IV-594 Me Me Me CH₂ Ph C(Me)₂ Et racemic IV-595 Me Me Me CH₂ Ph C(Me)₂ Et (S)- IV-596 Me Me Me CH₂ Ph C(Me)₂ cPr racemic IV-597 Me Me Me CH₂ Ph C(Me)₂ cPr (S)- IV-598 Me Me Me CH₂ Ph C(Me)₂ Ph racemic IV-599 Me Me Me CH₂ Ph C(Me)₂ Ph (S)- IV-600 Me Me Me CH₂ Ph (CH₂)₂ H racemic

TABLE 76 (IV)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁵ tion IV-601 Me Me Me CH₂ Ph (CH₂)₂ H (S)- IV-602 Me Et Me CH₂ Ph (CH₂)₂ H racemic IV-603 Me Et Me CH₂ Ph (CH₂)₂ H (S)- IV-604 Me Me Me CH₂ Ph (CH₂)₂ Me racemic IV-605 Me Me Me CH₂ Ph (CH₂)₂ Me (S)- IV-606 Me Et Me CH₂ Ph (CH₂)₂ Me racemic IV-607 Me Et Me CH₂ Ph (CH₂)₂ Me (S)- IV-608 Me Me Me CH₂ Ph (CH₂)₂ CHF₂ racemic IV-609 Me Me Me CH₂ Ph (CH₂)₂ CHF₂ (S)- IV-610 Me Me Me CH₂ Ph (CH₂)₂ Et racemic IV-611 Me Me Me CH₂ Ph (CH₂)₂ Et (S)- IV-612 Me Me Me CH₂ Ph (CH₂)₂ cPr racemic IV-613 Me Me Me CH₂ Ph (CH₂)₂ cPr (S)- IV-614 Me Me Me CH₂ Ph (CH₂)₂ Ph racemic IV-615 Me Me Me CH₂ Ph (CH₂)₂ Ph (S)- IV-616 Me Me Me CH₂ Ph CH₂C(Me)₂ H racemic IV-617 Me Me Me CH₂ Ph CH₂C(Me)₂ H (S)- IV-618 Me Et Me CH₂ Ph CH₂C(Me)₂ H racemic IV-619 Me Et Me CH₂ Ph CH₂C(Me)₂ H (S)- IV-620 Me Me Me CH₂ Ph CH₂C(Me)₂ Me racemic IV-621 Me Me Me CH₂ Ph CH₂C(Me)₂ Me (S)- IV-622 Me Et Me CH₂ Ph CH₂C(Me)₂ Me racemic IV-623 Me Et Me CH₂ Ph CH₂C(Me)₂ Me (S)- IV-624 Me Me Me CH₂ Ph CH₂C(Me)₂ CHF₂ racemic IV-625 Me Me Me CH₂ Ph CH₂C(Me)₂ CHF₂ (S)- IV-626 Me Me Me CH₂ Ph CH₂C(Me)₂ Et racemic IV-627 Me Me Me CH₂ Ph CH₂C(Me)₂ Et (S)- IV-628 Me Me Me CH₂ Ph CH₂C(Me)₂ cPr racemic IV-629 Me Me Me CH₂ Ph CH₂C(Me)₂ cPr (S)- IV-630 Me Me Me CH₂ Ph CH₂C(Me)₂ Ph racemic IV-631 Me Me Me CH₂ Ph CH₂C(Me)₂ Ph (S)- IV-632 Me Me Me — Ph CH₂ H racemic IV-633 Me Me Me — Ph CH₂ H (S)- IV-634 Me Me Me — Ph CH₂ Me racemic IV-635 Me Me Me — Ph CH₂ Me (S)- IV-636 Me Me Me CH═CH Ph CH₂ H racemic IV-637 Me Me Me CH═CH Ph CH₂ H (S)- IV-638 Me Me Me CH═CH Ph CH₂ Me racemic IV-639 Me Me Me CH═CH Ph CH₂ Me (S)- IV-640 Me Me Me C≡C Ph CH₂ H racemic IV-641 Me Me Me C≡C Ph CH₂ H (S)- IV-642 Me Me Me C≡C Ph CH₂ Me racemic IV-643 Me Me Me C≡C Ph CH₂ Me (S)- IV-644 Me Me Me 1,2-Cyclo- Ph CH₂ H racemic propylene IV-645 Me Me Me 1,2-Cyclo- Ph CH₂ H (S)- propylene IV-646 Me Me Me 1,2-Cyclo- Ph CH₂ Me racemic propylene IV-647 Me Me Me 1,2-Cyclo- Ph CH₂ Me (S)- propylene IV-648 Me Me Me 1,2-Cyclo Ph CH₂ H racemic propynylene IV-649 Me Me Me 1,2-Cyclo- Ph CH₂ H (S)- propynylene IV-650 Me Me Me 1,2-Cyclo- Ph CH₂ Me racemic propynylene IV-651 Me Me Me 1,2-Cyclo- Ph CH₂ Me (S)- propynylene

TABLE 77 (IV)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁵ tion IV-652 Me Me Me O Ph C(Me)₂CH₂ H racemic IV-653 Me Me Me O Ph C(Me)₂CH₂ H (+) IV-654 Me Me Me O Ph C(Me)₂CH₂ H (−) IV-655 Me Et Me O Ph C(Me)₂CH₂ H racemic IV-656 Me Et Me O Ph C(Me)₂CH₂ H (+) IV-657 Me Et Me O Ph C(Me)₂CH₂ H (−) IV-658 Me Me Me O Ph C(Me)₂CH₂ Me racemic IV-659 Me Me Me O Ph C(Me)₂CH₂ Me (+) IV-660 Me Me Me O Ph C(Me)₂CH₂ Me (−) IV-661 Me Et Me O Ph C(Me)₂CH₂ Me racemic IV-662 Me Et Me O Ph C(Me)₂CH₂ Me (+) IV-663 Me Et Me O Ph C(Me)₂CH₂ Me (−) IV-664 Me Me Me O Ph C(Me)₂CH₂ CHF₂ racemic IV-665 Me Me Me O Ph C(Me)₂CH₂ CHF₂ (+) IV-666 Me Me Me O Ph C(Me)₂CH₂ CHF₂ (−) IV-667 Me Me Me O Ph C(Me)₂CH₂ Et racemic IV-668 Me Me Me O Ph C(Me)₂CH₂ Et (+) IV-669 Me Me Me O Ph C(Me)₂CH₂ Et (−) IV-670 Me Me Me O H CH(Ph) H IV-671 Me Et Me O H CH(Ph) H IV-672 Me Me Me NH Ph C(Me)₂CH₂ H (+) IV-673 Me Me Me NH Ph C(Me)₂CH₂ H (−) IV-674 Me Et Me NH Ph C(Me)₂CH₂ H (+) IV-675 Me Et Me NH Ph C(Me)₂CH₂ H (−) IV-676 Me Me Me NH Ph C(Me)₂CH₂ Me racemic IV-677 Me Me Me NH Ph C(Me)₂CH₂ Me (+) IV-678 Me Me Me NH Ph C(Me)₂CH₂ Me (−) IV-679 Me Et Me NH Ph C(Me)₂CH₂ Me racemic IV-680 Me Et Me NH Ph C(Me)₂CH₂ Me (+) IV-681 Me Et Me NH Ph C(Me)₂CH₂ Me (−) IV-682 Me Me Me NH Ph C(Me)₂CH₂ CHF₂ racemic IV-683 Me Me Me NH Ph C(Me)₂CH₂ CHF₂ (+) IV-684 Me Me Me NH Ph C(Me)₂CH₂ CHF₂ (−) IV-685 Me Et Me NH Ph C(Me)₂CH₂ CHF₂ racemic IV-686 Me Et Me NH Ph C(Me)₂CH₂ CHF₂ (+) IV-687 Me Et Me NH Ph C(Me)₂CH₂ CHF₂ (−) IV-688 Me Me Me NH Ph C(Me)₂CH₂ Et racemic IV-689 Me Me Me NH Ph C(Me)₂CH₂ Et (+) IV-690 Me Me Me NH Ph C(Me)₂CH₂ Et (−) IV-691 Me Et Me NH Ph C(Me)₂CH₂ Et racemic IV-692 Me Et Me NH Ph C(Me)₂CH₂ Et (+) IV-693 Me Et Me NH Ph C(Me)₂CH₂ Et (−) IV-694 Me Me Me NH Ph C(Me)₂CH₂ iPr racemic IV-695 Me Me Me NH Ph C(Me)₂CH₂ iPr (+) IV-696 Me Me Me NH Ph C(Me)₂CH₂ iPr (−) IV-697 Me Et Me NH Ph C(Me)₂CH₂ iPr racemic IV-698 Me Et Me NH Ph C(Me)₂CH₂ iPr (+) IV-699 Me Et Me NH Ph C(Me)₂CH₂ iPr (−) IV-700 Me Me Me NH Ph C(Me)₂CH₂ cPr racemic IV-701 Me Me Me NH Ph C(Me)₂CH₂ cPr (+)

TABLE 78 (IV)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁵ tion IV-702 Me Me Me NH Ph C(Me)₂CH₂ cPr (−) IV-703 Me Et Me NH Ph C(Me)₂CH₂ cPr racemic IV-704 Me Et Me NH Ph C(Me)₂CH₂ cPr (+) IV-705 Me Et Me NH Ph C(Me)₂CH₂ cPr (−) IV-706 Me Me Me NH Ph 1,1-Cyclo- H racemic propylene- CH₂ IV-707 Me Me Me NH Ph 1,1-Cyclo- H (+) propylene- CH₂ IV-708 Me Me Me NH Ph 1,1-Cyclo- H (+) propylene- CH₂ IV-709 Me Et Me NH Ph 1,1-Cyclo- H racemic propylene- CH₂ IV-710 Me Et Me NH Ph 1,1-Cyclo- H (+) propylene- CH₂ IV-711 Me Et Me NH Ph 1,1-Cyclo- H (−) propylene- CH₂ IV-712 Me Me Me NH Ph 1,1-Cyclo- Me racemic propylene- CH₂ IV-713 Me Me Me NH Ph 1,1-Cyclo- Me (+) propylene- CH₂ IV-714 Me Me Me NH Ph 1,1-Cyclo- Me (−) propylene- CH₂ IV-715 Me Et Me NH Ph 1,1-Cyclo- Me racemic propylene- CH₂ IV-716 Me Et Me NH Ph 1,1-Cyclo- Me (+) propylene- CH₂ IV-717 Me Et Me NH Ph 1,1-Cyclo- Me (−) propylene- CH₂ IV-718 Me Me Me NH Ph 1,1-Cyclo- H racemic butylene- CH₂ IV-719 Me Me Me NH Ph 1,1-Cyclo- H (+) butylene- CH₂ IV-720 Me Me Me NH Ph 1,1-Cyclo- H (−) butylene- CH₂ IV-721 Me Et Me NH Ph 1,1-Cyclo- H racemic butylene- CH₂ IV-722 Me Et Me NH Ph 1,1-Cyclo- H (+) butylene- CH₂ IV-723 Me Et Me NH Ph 1,1-Cyclo- H (−) butylene- CH₂ IV-724 Me Me Me NH Ph 1,1-Cyclo- Me racemic butylene- CH₂ IV-725 Me Me Me NH Ph 1,1-Cyclo- Me (+) butylene- CH₂ IV-726 Me Me Me NH Ph 1,1-Cyclo- Me (−) butylene- CH₂ IV-727 Me Et Me NH Ph 1,1-Cyclo- Me racemic butylene- CH₂ IV-728 Me Et Me NH Ph 1,1-Cyclo- Me (+) butylene- CH₂ IV-729 Me Et Me NH Ph 1,1-Cyclo- Me (−) butylene- CH₂ IV-730 Me Me Me NH Ph C(Et)₂CH₂ H racemic IV-731 Me Me Me NH Ph C(Et)₂CH₂ H (+) IV-732 Me Me Me NH Ph C(Et)₂CH₂ H (−) IV-733 Me Et Me NH Ph C(Et)₂CH₂ H racemic IV-734 Me Et Me NH Ph C(Et)₂CH₂ H (+) IV-735 Me Et Me NH Ph C(Et)₂CH₂ H (−) IV-736 Me Me Me NH Ph C(Et)₂CH₂ Me racemic IV-737 Me Me Me NH Ph C(Et)₂CH₂ Me (+) IV-738 Me Me Me NH Ph C(Et)₂CH₂ Me (−) IV-739 Me Et Me NH Ph C(Et)₂CH₂ Me racemic IV-740 Me Et Me NH Ph C(Et)₂CH₂ Me (+) IV-741 Me Et Me NH Ph C(Et)₂CH₂ Me (−) IV-742 Me Me Me NH Ph CH₂-1,1- H racemic Cyclo- propylene IV-743 Me Me Me NH Ph CH₂-1,1- H (R)- Cyclo- propylene IV-744 Me Et Me NH Ph CH₂-1,1- H racemic Cyclo- propylene IV-745 Me Et Me NH Ph CH₂-1,1- H (R)- Cyclo- propylene IV-746 Me Me Me NH Ph CH₂-1,1- Me racemic Cyclo- propylene IV-747 Me Me Me NH Ph CH₂-1,1- Me (R)- Cyclo- propylene IV-748 Me Et Me NH Ph CH₂-1,1- Me racemic Cyclo- propylene IV-749 Me Et Me NH Ph CH₂-1,1- Me (R)- Cyclo- propylene IV-750 Me Me Me NH Ph CH₂-1,1- H racemic cyclo- butylene IV-751 Me Me Me NH Ph CH₂-1,1- H (R)- cyclo- butylene

TABLE 79 (IV)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁵ tion IV-752 Me Et Me NH Ph CH₂-1,1- H racemic cyclo- butylene IV-753 Me Et Me NH Ph CH₂-1,1- H (R)- cyclo- butylene IV-754 Me Me Me NH Ph CH₂-1,1- Me racemic cyclo- butylene IV-755 Me Me Me NH Ph CH₂-1,1- Me (R)- cyclo- butylene IV-756 Me Et Me NH Ph CH₂-1,1- Me racemic cyclo- butylene IV-757 Me Et Me NH Ph CH₂-1,1- Me (R)- cyclo- butylene IV-758 Me Me Me NH Ph CH₂C(Et)₂ H racemic IV-759 Me Me Me NH Ph CH₂C(Et)₂ H (R)- IV-760 Me Et Me NH Ph CH₂C(Et)₂ H racemic IV-761 Me Et Me NH Ph CH₂C(Et)₂ H (R)- IV-762 Me Me Me NH Ph CH₂C(Et)₂ Me racemic IV-763 Me Me Me NH Ph CH₂C(Et)₂ Me (R)- IV-764 Me Et Me NH Ph CH₂C(Et)₂ Me racemic IV-765 Me Et Me NH Ph CH₂C(Et)₂ Me (R)- IV-766 Me Me Me NH Ph (R)-CH(Me) H (S)- IV-767 Me Me Me NH Ph (S)-CH(Me) H (S)- IV-768 Me Et Me NH Ph (R)-CH(Me) H (S)- IV-769 Me Et Me NH Ph (S)-CH(Me) H (S)- IV-770 Me Me Me NH Ph (R)-CH(iPr) H (S)- IV-771 Me Me Me NH Ph (S)-CH(iPr) H (S)- IV-772 Me Et Me NH Ph (R)-CH(iPr) H (S)- IV-773 Me Et Me NH Ph (S)-CH(iPr) H (S)- IV-774 Me Me Me NH Ph (R)-CH(Ph) H (S)- IV-775 Me Me Me NH Ph (S)-CH(Ph) H (S)- IV-776 Me Et Me NH Ph (R)-CH(Ph) H (S)- IV-777 Me Et Me NH Ph (S)-CH(Ph) H (S)- IV-778 Me Me Me NH H (R)-CH(Me) H IV-779 Me Me Me NH H (S)-CH(Me) H IV-780 Me Et Me NH H (R)-CH(Me) H IV-781 Me Et Me NH H (S)-CH(Me) H IV-782 Me Me Me NH H (R)-CH(iPr) H IV-783 Me Me Me NH H (S)-CH(iPr) H IV-784 Me Et Me NH H (R)-CH(iPr) H IV-785 Me Et Me NH H (S)-CH(iPr) H IV-786 Me Me Me NH H (R)-CH(Ph) H IV-787 Me Me Me NH H (S)-CH(Ph) H IV-788 Me Et Me NH H (R)-CH(Ph) H IV-789 Me Et Me NH H (S)-CH(Ph) H IV-790 Me Me Me NH Me (R)-CH(Me) H (S)- IV-791 Me Me Me NH Me (S)-CH(Me) H (S)- IV-792 Me Et Me NH Me (R)-CH(Me) H (S)- IV-793 Me Et Me NH Me (S)-CH(Me) H (S)- IV-794 Me Me Me NH Me (R)-CH(iPr) H (S)- IV-795 Me Me Me NH Me (S)-CH(iPr) H (S)- IV-796 Me Et Me NH Me (R)-CH(iPr) H (S)- IV-797 Me Et Me NH Me (S)-CH(iPr) H (S)- IV-798 Me Me Me NH Me (R)-CH(Ph) H (S)- IV-799 Me Me Me NH Me (S)-CH(Ph) H (S)- IV-800 Me Et Me NH Me (R)-CH(Ph) H (S)- IV-801 Me Et Me NH Me (S)-CH(Ph) H (S)-

TABLE 80 (IV)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁵ tion IV-802 Me Me Me NH iPr CH₂ Me racemic IV-803 Me Me Me NH iPr CH₂ Me (S)- IV-804 Me Et Me NH iPr CH₂ Me racemic IV-805 Me Et Me NH iPr CH₂ Me (S)- IV-806 Me Me Me NH iPr (CH₂)₂ H racemic IV-807 Me Me Me NH iPr (CH₂)₂ H (R)- IV-808 Me Et Me NH iPr (CH₂)₂ H racemic IV-809 Me Et Me NH iPr (CH₂)₂ H (R)- IV-810 Me Me Me NH iPr (CH₂)₂ Me racemic IV-811 Me Me Me NH iPr (CH₂)₂ Me (R)- IV-812 Me Et Me NH iPr (CH₂)₂ Me racemic IV-813 Me Et Me NH iPr (CH₂)₂ Me (R)- IV-814 Me Me Me NH iPr CH₂C(Me)₂ H racemic IV-815 Me Me Me NH iPr CH₂C(Me)₂ H (R)- IV-816 Me Et Me NH iPr CH₂C(Me)₂ H racemic IV-817 Me Et Me NH iPr CH₂C(Me)₂ H (R)- IV-818 Me Me Me NH iPr CH₂C(Me)₂ Me racemic IV-819 Me Me Me NH iPr CH₂C(Me)₂ Me (R)- IV-820 Me Et Me NH iPr CH₂C(Me)₂ Me racemic IV-821 Me Et Me NH iPr CH₂C(Me)₂ Me (R)- IV-822 Me Me Me NH iPr C(Me)₂CH₂ H racemic IV-823 Me Me Me NH iPr C(Me)₂CH₂ H (+) IV-824 Me Me Me NH iPr C(Me)₂CH₂ H (−) IV-825 Me Et Me NH iPr C(Me)₂CH₂ H racemic IV-826 Me Et Me NH iPr C(Me)₂CH₂ H (+) IV-827 Me Et Me NH iPr C(Me)₂CH₂ H (−) IV-828 Me Me Me NH iPr C(Me)₂CH₂ Me racemic IV-829 Me Me Me NH iPr C(Me)₂CH₂ Me (+) IV-830 Me Me Me NH iPr C(Me)₂CH₂ Me (−) IV-831 Me Et Me NH iPr C(Me)₂CH₂ Me racemic IV-832 Me Et Me NH iPr C(Me)₂CH₂ Me (+) IV-833 Me Et Me NH iPr C(Me)₂CH₂ Me (−) IV-834 Me Me Me NH iPr (R)-CH(Me) H (S)- IV-835 Me Me Me NH iPr (S)-CH(Me) H (S)- IV-836 Me Et Me NH iPr (R)-CH(Me) H (S)- IV-837 Me Et Me NH iPr (S)-CH(Me) H (S)- IV-838 Me Me Me NH iPr (R)-CH(iPr) H (S)- IV-839 Me Me Me NH iPr (S)-CH(iPr) H (S)- IV-840 Me Et Me NH iPr (R)-CH(iPr) H (S)- IV-841 Me Et Me NH iPr (S)-CH(iPr) H (S)- IV-842 Me Me Me NH iPr (R)-CH(Ph) H (S)- IV-843 Me Me Me NH iPr (S)-CH(Ph) H (S)- IV-844 Me Et Me NH iPr (R)-CH(Ph) H (S)- IV-845 Me Et Me NH iPr (S)-CH(Ph) H (S)- IV-846 Me Me Me NH CF₃ CH₂ H racemic IV-847 Me Me Me NH CF₃ CH₂ H (S)- IV-848 Me Et Me NH CF₃ CH₂ H racemic IV-849 Me Et Me NH CF₃ CH₂ H (S)- IV-850 Me Me Me N(Me) CF₃ CH₂ H racemic IV-851 Me Me Me N(Me) CF₃ CH₂ H (S)-

TABLE 81 (IV)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁵ tion IV-852 Me Et Me N(Me) CF₃ CH₂ H racemic IV-853 Me Et Me N(Me) CF₃ CH₂ H (S)- IV-854 Me Me Me NH CH₂OH CH₂ H IV-855 Me Et Me NH CH₂OH CH₂ H IV-856 Me Me Me NH CH₂OMe CH₂ H racemic IV-857 Me Me Me NH CH₂OMe CH₂ H (R)- IV-858 Me Et Me NH CH₂OMe CH₂ H racemic IV-859 Me Et Me NH CH₂OMe CH₂ H (R)- IV-860 Me Me Me NH CH₂Ph CH₂ H racemic IV-861 Me Me Me NH CH₂Ph CH₂ H (R)- IV-862 Me Me Me NH CH₂Ph CH₂ H (S)- IV-863 Me Et Me NH CH₂Ph CH₂ H racemic IV-864 Me Et Me NH CH₂Ph CH₂ H (S)- IV-865 Me Me Me N(Me) CH₂Ph CH₂ H racemic IV-866 Me Me Me N(Me) CH₂Ph CH₂ H (S)- IV-867 Me Et Me N(Me) CH₂Ph CH₂ H racemic IV-868 Me Et Me N(Me) CH₂Ph CH₂ H (S)- IV-869 Me Me Me NH 2-F—Ph CH₂ Me racemic IV-870 Me Me Me NH 2-F—Ph CH₂ Me (S)- IV-871 Me Et Me NH 2-F—Ph CH₂ Me racemic IV-872 Me Et Me NH 2-F—Ph CH₂ Me (S)- IV-873 Me Me Me NH 2-F—Ph (CH₂)₂ H racemic IV-874 Me Me Me NH 2-F—Ph (CH₂)₂ H (+)- IV-875 Me Me Me NH 2-F—Ph (CH₂)₂ H (−)- IV-876 Me Et Me NH 2-F—Ph (CH₂)₂ H racemic IV-877 Me Et Me NH 2-F—Ph (CH₂)₂ H (R)- IV-878 Me Me Me NH 2-F—Ph (CH₂)₂ Me racemic IV-879 Me Me Me NH 2-F—Ph (CH₂)₂ Me (R)- IV-880 Me Et Me NH 2-F—Ph (CH₂)₂ Me racemic IV-881 Me Et Me NH 2-F—Ph (CH₂)₂ Me (R)- IV-882 Me Me Me NH 2-F—Ph CH₂C(Me)₂ H racemic IV-883 Me Me Me NH 2-F—Ph CH₂C(Me)₂ H (R)- IV-884 Me Et Me NH 2-F—Ph CH₂C(Me)₂ H racemic IV-885 Me Et Me NH 2-F—Ph CH₂C(Me)₂ H (R)- IV-886 Me Me Me NH 2-F—Ph CH₂C(Me)₂ Me racemic IV-887 Me Me Me NH 2-F—Ph CH₂C(Me)₂ Me (R)- IV-888 Me Et Me NH 2-F—Ph CH₂C(Me)₂ Me racemic IV-889 Me Et Me NH 2-F—Ph CH₂C(Me)₂ Me (R)- IV-890 Me Me Me NH 2-F—Ph C(Me)₂CH₂ H racemic IV-891 Me Me Me NH 2-F—Ph C(Me)₂CH₂ H (+) IV-892 Me Me Me NH 2-F—Ph C(Me)₂CH₂ H (−) IV-893 Me Et Me NH 2-F—Ph C(Me)₂CH₂ H racemic IV-894 Me Et Me NH 2-F—Ph C(Me)₂CH₂ H (+) IV-895 Me Et Me NH 2-F—Ph C(Me)₂CH₂ H (−) IV-896 Me Me Me NH 2-F—Ph C(Me)₂CH₂ Me racemic IV-897 Me Me Me NH 2-F—Ph C(Me)₂CH₂ Me (+) IV-898 Me Me Me NH 2-F—Ph C(Me)₂CH₂ Me (−) IV-899 Me Et Me NH 2-F—Ph C(Me)₂CH₂ Me racemic IV-900 Me Et Me NH 2-F—Ph C(Me)₂CH₂ Me (+) IV-901 Me Et Me NH 2-F—Ph C(Me)₂CH₂ Me (−)

TABLE 82 (IV)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁵ tion IV-902 Me Me Me NH 3-F—Ph (CH₂)₂ H racemic IV-903 Me Me Me NH 3-F—Ph (CH₂)₂ H (R)- IV-904 Me Et Me NH 3-F—Ph (CH₂)₂ H racemic IV-905 Me Et Me NH 3-F—Ph (CH₂)₂ H (R)- IV-906 Me Me Me NH 3-F—Ph (CH₂)₂ Me racemic IV-907 Me Me Me NH 3-F—Ph (CH₂)₂ Me (R)- IV-908 Me Et Me NH 3-F—Ph (CH₂)₂ Me racemic IV-909 Me Et Me NH 3-F—Ph (CH₂)₂ Me (R)- IV-910 Me Me Me NH 3-F—Ph CH₂C(Me)₂ H racemic IV-911 Me Me Me NH 3-F—Ph CH₂C(Me)₂ H (R)- IV-912 Me Et Me NH 3-F—Ph CH₂C(Me)₂ H racemic IV-913 Me Et Me NH 3-F—Ph CH₂C(Me)₂ H (R)- IV-914 Me Me Me NH 3-F—Ph CH₂C(Me)₂ Me racemic IV-915 Me Me Me NH 3-F—Ph CH₂C(Me)₂ Me (R)- IV-916 Me Et Me NH 3-F—Ph CH₂C(Me)₂ Me racemic IV-917 Me Et Me NH 3-F—Ph CH₂C(Me)₂ Me (R)- IV-918 Me Me Me NH 3-F—Ph C(Me)₂CH₂ H racemic IV-919 Me Me Me NH 3-F—Ph C(Me)₂CH₂ H (+) IV-920 Me Me Me NH 3-F—Ph C(Me)₂CH₂ H (−) IV-921 Me Et Me NH 3-F—Ph C(Me)₂CH₂ H racemic IV-922 Me Et Me NH 3-F—Ph C(Me)₂CH₂ H (+) IV-923 Me Et Me NH 3-F—Ph C(Me)₂CH₂ H (−) IV-924 Me Me Me NH 3-F—Ph C(Me)₂CH₂ Me racemic IV-925 Me Me Me NH 3-F—Ph C(Me)₂CH₂ Me (+) IV-926 Me Me Me NH 3-F—Ph C(Me)₂CH₂ Me (−) IV-927 Me Et Me NH 3-F—Ph C(Me)₂CH₂ Me racemic IV-928 Me Et Me NH 3-F—Ph C(Me)₂CH₂ Me (+) IV-929 Me Et Me NH 3-F—Ph C(Me)₂CH₂ Me (−) IV-930 Me Me Me NH 4-F—Ph (CH₂)₂ H racemic IV-931 Me Me Me NH 4-F—Ph (CH₂)₂ H (R)- IV-932 Me Et Me NH 4-F—Ph (CH₂)₂ H racemic IV-933 Me Et Me NH 4-F—Ph (CH₂)₂ H (R)- IV-934 Me Me Me NH 4-F—Ph (CH₂)₂ Me racemic IV-935 Me Me Me NH 4-F—Ph (CH₂)₂ Me (R)- IV-936 Me Et Me NH 4-F—Ph (CH₂)₂ Me racemic IV-937 Me Et Me NH 4-F—Ph (CH₂)₂ Me (R)- IV-938 Me Me Me NH 4-F—Ph CH₂C(Me)₂ H racemic IV-939 Me Me Me NH 4-F—Ph CH₂C(Me)₂ H (R)- IV-940 Me Et Me NH 4-F—Ph CH₂C(Me)₂ H racemic IV-941 Me Et Me NH 4-F—Ph CH₂C(Me)₂ H (R)- IV-942 Me Me Me NH 4-F—Ph CH₂C(Me)₂ Me racemic IV-943 Me Me Me NH 4-F—Ph CH₂C(Me)₂ Me (R)- IV-944 Me Et Me NH 4-F—Ph CH₂C(Me)₂ Me racemic IV-945 Me Et Me NH 4-F—Ph CH₂C(Me)₂ Me (R)- IV-946 Me Me Me NH 4-F—Ph C(Me)₂CH₂ H racemic IV-947 Me Me Me NH 4-F—Ph C(Me)₂CH₂ H (+) IV-948 Me Me Me NH 4-F—Ph C(Me)₂CH₂ H (−) IV-949 Me Et Me NH 4-F—Ph C(Me)₂CH₂ H racemic IV-950 Me Et Me NH 4-F—Ph C(Me)₂CH₂ H (+) IV-951 Me Et Me NH 4-F—Ph C(Me)₂CH₂ H (−)

TABLE 83 (IV)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁵ tion IV-952 Me Me Me NH 4-F—Ph C(Me)₂CH₂ Me racemic IV-953 Me Me Me NH 4-F—Ph C(Me)₂CH₂ Me (+) IV-954 Me Me Me NH 4-F—Ph C(Me)₂CH₂ Me (−) IV-955 Me Et Me NH 4-F—Ph C(Me)₂CH₂ Me racemic IV-956 Me Et Me NH 4-F—Ph C(Me)₂CH₂ Me (+) IV-957 Me Et Me NH 4-F—Ph C(Me)₂CH₂ Me (−) IV-958 Me Me Me NH 2-Cl—Ph CH₂ H racemic IV-959 Me Me Me NH 2-Cl—Ph CH₂ H (S)- IV-960 Me Et Me NH 2-Cl—Ph CH₂ H racemic IV-961 Me Et Me NH 2-Cl—Ph CH₂ H (S)- IV-962 Me Me Me NH 2-Cl—Ph CH₂ Me racemic IV-963 Me Me Me NH 2-Cl—Ph CH₂ Me (S)- IV-964 Me Et Me NH 2-Cl—Ph CH₂ Me racemic IV-965 Me Et Me NH 2-Cl—Ph CH₂ Me (S)- IV-966 Me Me Me NH 2-Cl—Ph (CH₂)₂ H racemic IV-967 Me Me Me NH 2-Cl—Ph (CH₂)₂ H (R)- IV-968 Me Et Me NH 2-Cl—Ph (CH₂)₂ H racemic IV-969 Me Et Me NH 2-Cl—Ph (CH₂)₂ H (R)- IV-970 Me Me Me NH 2-Cl—Ph (CH₂)₂ Me racemic IV-971 Me Me Me NH 2-Cl—Ph (CH₂)₂ Me (R)- IV-972 Me Et Me NH 2-Cl—Ph (CH₂)₂ Me racemic IV-973 Me Et Me NH 2-Cl—Ph (CH₂)₂ Me (R)- IV-974 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ H racemic IV-975 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ H (R)- IV-976 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ H racemic IV-977 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ H (R)- IV-978 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ Me racemic IV-979 Me Me Me NH 2-Cl—Ph CH₂C(Me)₂ Me (R)- IV-980 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ Me racemic IV-981 Me Et Me NH 2-Cl—Ph CH₂C(Me)₂ Me (R)- IV-982 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ H racemic IV-983 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ H (+) IV-984 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ H (−) IV-985 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ H racemic IV-986 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ H (+) IV-987 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ H (−) IV-988 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ Me racemic IV-989 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ Me (+) IV-990 Me Me Me NH 2-Cl—Ph C(Me)₂CH₂ Me (−) IV-991 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ Me racemic IV-992 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ Me (+) IV-993 Me Et Me NH 2-Cl—Ph C(Me)₂CH₂ Me (−) IV-994 Me Me Me NH 3-Cl—Ph CH₂ H racemic IV-995 Me Me Me NH 3-Cl—Ph CH₂ H (S)- IV-996 Me Et Me NH 3-Cl—Ph CH₂ H racemic IV-997 Me Et Me NH 3-Cl—Ph CH₂ H (S)- IV-998 Me Me Me NH 3-Cl—Ph CH₂ Me racemic IV-999 Me Me Me NH 3-Cl—Ph CH₂ Me (S)- IV-1000 Me Et Me NH 3-Cl—Ph CH₂ Me racemic IV-1001 Me Et Me NH 3-Cl—Ph CH₂ Me (S)-

TABLE 84 (IV)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration IV-1002 Me Me Me NH 3-Cl—Ph (CH₂)₂ H racemic IV-1003 Me Me Me NH 3-Cl—Ph (CH₂)₂ H (R)- IV-1004 Me Et Me NH 3-Cl—Ph (CH₂)₂ H racemic IV-1005 Me Et Me NH 3-Cl—Ph (CH₂)₂ H (R)- IV-1006 Me Me Me NH 3-Cl—Ph (CH₂)₂ Me racemic IV-1007 Me Me Me NH 3-Cl—Ph (CH₂)₂ Me (R)- IV-1008 Me Et Me NH 3-Cl—Ph (CH₂)₂ Me racemic IV-1009 Me Et Me NH 3-Cl—Ph (CH₂)₂ Me (R)- IV-1010 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ H racemic IV-1011 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ H (R)- IV-1012 Me Et Me NH 3-Cl—Ph CH₂C(Me)₂ H racemic IV-1013 Me Et Me NH 3-Cl—Ph CH₂C(Me)₂ H (R)- IV-1014 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ Me racemic IV-1015 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ Me (R)- IV-1016 Me Et Me NH 3-Cl—Ph CH₂C(Me)₂ Me racemic IV-1017 Me Et Me NH 3-Cl—Ph CH₂C(Me)₂ Me (R)- IV-1018 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ H racemic IV-1019 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ H (+) IV-1020 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ H (−) IV-1021 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ H racemic IV-1022 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ H (+30) IV-1023 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ H (-) IV-1024 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ Me racemic IV-1025 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ Me (+) IV-1026 Me Me Me NH 3-Cl—Ph C(Me)₂CH₂ Me (−) IV-1027 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ Me racemic IV-1028 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ Me (+) IV-1029 Me Et Me NH 3-Cl—Ph C(Me)₂CH₂ Me (−) IV-1030 Me Me Me NH 3-Cl—Ph CH₂ H racemic IV-1031 Me Me Me NH 3-Cl—Ph CH₂ H (S)- IV-1032 Me Et Me NH 3-Cl—Ph CH₂ H racemic IV-1033 Me Et Me NH 3-Cl—Ph CH₂ H (S)- IV-1034 Me Me Me NH 3-Cl—Ph CH₂ Me racemic IV-1035 Me Me Me NH 3-Cl—Ph CH₂ Me (S)- IV-1036 Me Et Me NH 3-Cl—Ph CH₂ Me racemic IV-1037 Me Et Me NH 3-Cl—Ph CH₂ Me (S)- IV-1038 Me Me Me NH 3-Cl—Ph (CH₂)₂ H racemic IV-1039 Me Me Me NH 3-Cl—Ph (CH₂)₂ H (R)- IV-1040 Me Et Me NH 3-Cl—Ph (CH₂)₂ H racemic IV-1041 Me Et Me NH 3-Cl—Ph (CH₂)₂ H (R)- IV-1042 Me Me Me NH 3-Cl—Ph (CH₂)₂ Me racemic IV-1043 Me Me Me NH 3-Cl—Ph (CH₂)₂ Me (R)- IV-1044 Me Et Me NH 3-Cl—Ph (CH₂)₂ Me racemic IV-1045 Me Et Me NH 3-Cl—Ph (CH₂)₂ Me (R)- IV-1046 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ H racemic IV-1047 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ H (R)- IV-1048 Me Et Me NH 3-Cl—Ph CH₂C(Me)₂ H racemic IV-1049 Me Et Me NH 3-Cl—Ph CH₂C(Me)₂ H (R)- IV-1050 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ Me racemic IV-1051 Me Me Me NH 3-Cl—Ph CH₂C(Me)₂ Me (R)-

TABLE 85 (IV)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration IV-1052 Me Et Me NH 4-Cl—Ph CH₂C(Me)₂ Me racemic IV-1053 Me Et Me NH 4-Cl—Ph CH₂C(Me)₂ Me (R)- IV-1054 Me Me Me NH 4-Cl—Ph CH₂C(Me)₂ H racemic IV-1055 Me Me Me NH 4-Cl—Ph CH₂C(Me)₂ H (+) IV-1056 Me Me Me NH 4-Cl—Ph CH₂C(Me)₂ H (−) IV-1057 Me Et Me NH 4-Cl—Ph CH₂C(Me)₂ H racemic IV-1058 Me Et Me NH 4-Cl—Ph CH₂C(Me)₂ H (+) IV-1059 Me Et Me NH 4-Cl—Ph CH₂C(Me)₂ H (−) IV-1060 Me Me Me NH 4-Cl—Ph CH₂C(Me)₂ Me racemic IV-1061 Me Me Me NH 4-Cl—Ph CH₂C(Me)₂ Me (+) IV-1062 Me Me Me NH 4-Cl—Ph CH₂C(Me)₂ Me (−) IV-1063 Me Et Me NH 4-Cl—Ph CH₂C(Me)₂ Me racemic IV-1064 Me Et Me NH 4-Cl—Ph CH₂C(Me)₂ Me (+) IV-1065 Me Et Me NH 4-Cl—Ph CH₂C(Me)₂ Me (−) IV-1066 Me Me Me NH 2-Me—Ph CH₂ H racemic IV-1067 Me Me Me NH 2-Me—Ph CH₂ H (S)- IV-1068 Me Et Me NH 2-Me—Ph CH₂ H racemic IV-1069 Me Et Me NH 2-Me—Ph CH₂ H (S)- IV-1070 Me Me Me NH 2-Me—Ph CH₂ Me racemic IV-1071 Me Me Me NH 2-Me—Ph CH₂ Me (S)- IV-1072 Me Et Me NH 2-Me—Ph CH₂ Me racemic IV-1073 Me Et Me NH 2-Me—Ph CH₂ Me (S)- IV-1074 Me Me Me NH 2-Me—Ph (CH₂)₂ H racemic IV-1075 Me Me Me NH 2-Me—Ph (CH₂)₂ H (R)- IV-1076 Me Et Me NH 2-Me—Ph (CH₂)₂ H racemic IV-1077 Me Et Me NH 2-Me—Ph (CH₂)₂ H (R)- IV-1078 Me Me Me NH 2-Me—Ph (CH₂)₂ Me racemic IV-1079 Me Me Me NH 2-Me—Ph (CH₂)₂ Me (R)- IV-1080 Me Et Me NH 2-Me—Ph (CH₂)₂ Me racemic IV-1081 Me Et Me NH 2-Me—Ph (CH₂)₂ Me (R)- IV-1082 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ H racemic IV-1083 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ H (R)- IV-1084 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ H racemic IV-1085 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ H (R)- IV-1086 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ Me racemic IV-1087 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ Me (R)- IV-1088 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ Me racemic IV-1089 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ Me (R)- IV-1090 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ H racemic IV-1091 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ H (+) IV-1092 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ H (−) IV-1093 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ H racemic IV-1094 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ H (+) IV-1095 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ H (−) IV-1096 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ Me racemic IV-1097 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ Me (+) IV-1098 Me Me Me NH 2-Me—Ph CH₂C(Me)₂ Me (−) IV-1099 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ Me racemic IV-1100 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ Me (+) IV-1101 Me Et Me NH 2-Me—Ph CH₂C(Me)₂ Me (−)

TABLE 86 (IV)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration IV-1102 Me Me Me NH 3-Me—Ph CH₂ H racemic IV-1103 Me Me Me NH 3-Me—Ph CH₂ H (S)- IV-1104 Me Et Me NH 3-Me—Ph CH₂ H racemic IV-1105 Me Et Me NH 3-Me—Ph CH₂ H (S)- IV-1106 Me Me Me NH 3-Me—Ph CH₂ Me racemic IV-1107 Me Me Me NH 3-Me—Ph CH₂ Me (S)- IV-1108 Me Et Me NH 3-Me—Ph CH₂ Me racemic IV-1109 Me Et Me NH 3-Me—Ph CH₂ Me (S)- IV-1110 Me Me Me NH 3-Me—Ph (CH₂)₂ H racemic IV-1111 Me Me Me NH 3-Me—Ph (CH₂)₂ H (R)- IV-1112 Me Et Me NH 3-Me—Ph (CH₂)₂ H racemic IV-1113 Me Et Me NH 3-Me—Ph (CH₂)₂ H (R)- IV-1114 Me Me Me NH 3-Me—Ph (CH₂)₂ Me racemic IV-1115 Me Me Me NH 3-Me—Ph (CH₂)₂ Me (R)- IV-1116 Me Et Me NH 3-Me—Ph (CH₂)₂ Me racemic IV-1117 Me Et Me NH 3-Me—Ph (CH₂)₂ Me (R)- IV-1118 Me Me Me NH 3-Me—Ph CH₂C(Me)₂ H racemic IV-1119 Me Me Me NH 3-Me—Ph CH₂C(Me)₂ H (R)- IV-1120 Me Et Me NH 3-Me—Ph CH₂C(Me)₂ H racemic IV-1121 Me Et Me NH 3-Me—Ph CH₂C(Me)₂ H (R)- IV-1122 Me Me Me NH 3-Me—Ph CH₂C(Me)₂ Me racemic IV-1123 Me Me Me NH 3-Me—Ph CH₂C(Me)₂ Me (R)- IV-1124 Me Et Me NH 3-Me—Ph CH₂C(Me)₂ Me racemic IV-1125 Me Et Me NH 3-Me—Ph CH₂C(Me)₂ Me (R)- IV-1126 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ H racemic IV-1127 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ H (+) IV-1128 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ H (−) IV-1129 Me Et Me NH 3-Me—Ph C(Me)₂CH₂ H racemic IV-1130 Me Et Me NH 3-Me—Ph C(Me)₂CH₂ H (+) IV-1131 Me Et Me NH 3-Me—Ph C(Me)₂CH₂ H (−) IV-1132 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ Me racemic IV-1133 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ Me (+) IV-1134 Me Me Me NH 3-Me—Ph C(Me)₂CH₂ Me (−) IV-1135 Me Et Me NH 3-Me—Ph C(Me)₂CH₂ Me racemic IV-1136 Me Et Me NH 3-Me—Ph C(Me)₂CH₂ Me (+) IV-1137 Me Et Me NH 3-Me—Ph C(Me)₂CH₂ Me (−) IV-1138 Me Me Me NH 3-Me—Ph CH₂ H racemic IV-1139 Me Me Me NH 3-Me—Ph CH₂ H (S)- IV-1140 Me Et Me NH 3-Me—Ph CH₂ H racemic IV-1141 Me Et Me NH 3-Me—Ph CH₂ H (S)- IV-1142 Me Me Me NH 3-Me—Ph CH₂ Me racemic IV-1143 Me Me Me NH 3-Me—Ph CH₂ Me (S)- IV-1144 Me Et Me NH 3-Me—Ph CH₂ Me racemic IV-1145 Me Et Me NH 3-Me—Ph CH₂ Me (S)- IV-1146 Me Me Me NH 3-Me—Ph (CH₂)₂ H racemic IV-1147 Me Me Me NH 3-Me—Ph (CH₂)₂ H (R)- IV-1148 Me Me Me NH 3-Me—Ph (CH₂)₂ Me racemic IV-1149 Me Me Me NH 3-Me—Ph (CH₂)₂ Me (R)- IV-1150 Me Me Me NH 3-Me—Ph CH₂C(Me)₂ H racemic IV-1151 Me Me Me NH 3-Me—Ph CH₂C(Me)₂ H (R)-

TABLE 87 (IV)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration IV-1152 Me Et Me NH 4-Me—Ph CH₂C(Me)₂ H racemic IV-1153 Me Et Me NH 4-Me—Ph CH₂C(Me)₂ H (R)- IV-1154 Me Me Me NH 4-Me—Ph CH₂C(Me)₂ Me racemic IV-1155 Me Me Me NH 4-Me—Ph CH₂C(Me)₂ Me (R)- IV-1156 Me Et Me NH 4-Me—Ph CH₂C(Me)₂ Me racemic IV-1157 Me Et Me NH 4-Me—Ph CH₂C(Me)₂ Me (R)- IV-1158 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ H racemic IV-1159 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ H (+) IV-1160 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ H (−) IV-1161 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ H racemic IV-1162 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ H (+) IV-1163 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ H (−) IV-1164 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ Me racemic IV-1165 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ Me (+) IV-1166 Me Me Me NH 4-Me—Ph C(Me)₂CH₂ Me (−) IV-1167 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ Me racemic IV-1168 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ Me (+) IV-1169 Me Et Me NH 4-Me—Ph C(Me)₂CH₂ Me (−) IV-1170 Me Me Me — Ph — H racemic IV-1171 Me Me Me — Ph — H (R)- IV-1172 Me Et Me — Ph — H racemic IV-1173 Me Et Me — Ph — H (R)- IV-1174 Me Me Me — Ph — Me racemic IV-1175 Me Me Me — Ph — Me (R)- IV-1176 Me Me Me — Ph — Me (S)- IV-1177 Me Et Me — Ph — Me racemic IV-1178 Me Et Me — Ph — Me (R)- IV-1179 Me Me Me — Ph — CHF₂ racemic IV-1180 Me Me Me — Ph — CHF₂ (R)- IV-1181 Me Et Me — Ph — CHF₂ racemic IV-1182 Me Et Me — Ph — CHF₂ (R)- IV-1183 Me Me Me — Ph — CF₃ racemic IV-1184 Me Me Me — Ph — CF₃ (R)- IV-1185 Me Et Me — Ph — CF₃ racemic IV-1186 Me Et Me — Ph — CF₃ (R)- IV-1187 Me Me Me — Ph — Et racemic IV-1188 Me Me Me — Ph — Et (R)- IV-1189 Me Et Me — Ph — Et racemic IV-1190 Me Et Me — Ph — Et (R)- IV-1191 Me Me Me — Ph — CF₂CH₃ racemic IV-1192 Me Me Me — Ph — CF₂CH₃ (R)- IV-1193 Me Et Me — Ph — CF₂CH₃ racemic IV-1194 Me Et Me — Ph — CF₂CH₃ (R)- IV-1195 Me Me Me — Ph — nPr racemic IV-1196 Me Me Me — Ph — nPr (R)- IV-1197 Me Et Me — Ph — nPr racemic IV-1198 Me Et Me — Ph — nPr (R)- IV-1199 Me Me Me — Ph — nBu racemic IV-1200 Me Me Me — Ph — nBu (R)- IV-1201 Me Et Me — Ph — nBu racemic

TABLE 88 (IV)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration IV-1202 Me Et Me — Ph — nBu (R)- IV-1203 Me Me Me — Ph — iPr racemic IV-1204 Me Me Me — Ph — iPr (R)- IV-1205 Me Et Me — Ph — iPr racemic IV-1206 Me Et Me — Ph — iPr (R)- IV-1207 Me Me Me — Ph — cPr racemic IV-1208 Me Me Me — Ph — cPr (R)- IV-1209 Me Et Me — Ph — cPr racemic IV-1210 Me Et Me — Ph — cPr (R)- IV-1211 Me Me Me — Ph — Ph racemic IV-1212 Me Me Me — Ph — Ph (R)- IV-1213 Me Me Me — Ph — 2,2-diF-cPr racemic IV-1214 Me Me Me — Ph — 2,2-diF-cPr (R)- IV-1215 Me Me Me — Ph CH₂ H (R)- IV-1216 Me Me Me — Ph CH₂ CHF₂ racemic IV-1217 Me Me Me — Ph CH₂ CHF₂ (S)- IV-1218 Me Me Me — Ph CH₂ Et racemic IV-1219 Me Me Me — Ph CH₂ Et (S)- IV-1220 Me Me Me — Ph CH₂ Bn racemic IV-1221 Me Me Me — Ph CH₂ Bn (R)- IV-1222 Me Me Me — Ph (CH₂)₂ H racemic IV-1223 Me Me Me — Ph (CH₂)₂ H (S)- IV-1224 Me Me Me — Ph (CH₂)₂ Me racemic IV-1225 Me Me Me — Ph (CH₂)₂ Me (S)- IV-1226 Me Me Me — Ph (CH₂)₂ CHF₂ racemic IV-1227 Me Me Me — Ph (CH₂)₂ CHF₂ (S)- IV-1228 Me Me Me — Ph (CH₂)₂ Et racemic IV-1229 Me Me Me — Ph (CH₂)₂ Et (S)- IV-1230 Me Me Me — H — H IV-1231 Me Me Me — H — Me IV-1232 Me Me Me — H — CHF₂ IV-1233 Me Me Me — H — CF₃ IV-1234 Me Me Me — H — Et IV-1235 Me Me Me — H — nPr IV-1236 Me Me Me — H — iPr IV-1237 Me Me Me — H — cPr IV-1238 Me Me Me — H — Ph IV-1239 Me Me Me — Me — H racemic IV-1240 Me Me Me — Me — H (R)- IV-1241 Me Me Me — Me — Me racemic IV-1242 Me Me Me — Me — Me (R)- IV-1243 Me Me Me — Me — CHF₂ racemic IV-1244 Me Me Me — Me — CHF₂ (R)- IV-1245 Me Me Me — Me — CF₃ racemic IV-1246 Me Me Me — Me — CF₃ (R)- IV-1247 Me Me Me — Me — Et racemic IV-1248 Me Me Me — Me — Et (R)- IV-1249 Me Me Me — Me — nPr racemic IV-1250 Me Me Me — Me — nPr (R)- IV-1251 Me Me Me — Me — iPr racemic

TABLE 89 (IV)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration IV-1252 Me Me Me — Me — iPr (R)- IV-1253 Me Me Me — Me — cPr racemic IV-1254 Me Me Me — Me — cPr (R)- IV-1255 Me Me Me — Me — cHex racemic IV-1256 Me Me Me — Me — cHex (R)- IV-1257 Me Me Me — Me — Ph racemic IV-1258 Me Me Me — Me — Ph (R)- IV-1259 Me Me Me — Me — Ph (S)- IV-1260 Me Me Me — Me — 2-F—Ph racemic IV-1261 Me Me Me — Me — 2-F—Ph (R)- IV-1262 Me Me Me — Me — 2-F—Ph racemic IV-1263 Me Me Me — Me — 2-F—Ph (R)- IV-1264 Me Me Me — Me — 2-F—Ph racemic IV-1265 Me Me Me — Me — 2-F—Ph (R)- IV-1266 Me Me Me — Me — 2-Cl—Ph racemic IV-1267 Me Me Me — Me — 2-Cl—Ph (R)- IV-1268 Me Me Me — Me — 2-Cl—Ph racemic IV-1269 Me Me Me — Me — 2-Cl—Ph (R)- IV-1270 Me Me Me — Me — 2-Cl—Ph racemic IV-1271 Me Me Me — Me — 2-Cl—Ph (R)- IV-1272 Me Me Me — Me — 2-Py racemic IV-1273 Me Me Me — Me — 2-Py (R)- IV-1274 Me Me Me — Me — 3-Py racemic IV-1275 Me Me Me — Me — 3-Py (R)- IV-1276 Me Me Me — Me — 4-Py racemic IV-1277 Me Me Me — Me — 4-Py (R)- IV-1278 Me Me Me — iPr — H racemic IV-1279 Me Me Me — iPr — H (R)- IV-1280 Me Me Me — iPr — Me racemic IV-1281 Me Me Me — iPr — Me (R)- IV-1282 Me Me Me — iPr — CHF₂ racemic IV-1283 Me Me Me — iPr — CHF₂ (R)- IV-1284 Me Me Me — iPr — CF₃ racemic IV-1285 Me Me Me — iPr — CF₃ (R)- IV-1286 Me Me Me — iPr — Et racemic IV-1287 Me Me Me — iPr — Et (R)- IV-1288 Me Me Me — iPr — nPr racemic IV-1289 Me Me Me — iPr — nPr (R)- IV-1290 Me Me Me — iPr — iPr racemic IV-1291 Me Me Me — iPr — iPr (R)- IV-1292 Me Me Me — iPr — cPr racemic IV-1293 Me Me Me — iPr — cPr (R)- IV-1294 Me Me Me — iPr — Ph racemic IV-1295 Me Me Me — iPr — Ph (R)- IV-1296 Me Me Me — CF₃ — H racemic IV-1297 Me Me Me — CF₃ — H (R)- IV-1298 Me Me Me — CF₃ — Me racemic IV-1299 Me Me Me — CF₃ — Me (R)- IV-1300 Me Me Me — CF₃ — CHF₂ racemic IV-1301 Me Me Me — CF₃ — CHF₂ (R)-

TABLE 90 (IV)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration IV-1302 Me Me Me — CF₃ — CF₃ racemic IV-1303 Me Me Me — CF₃ — CF₃ (R)- IV-1304 Me Me Me — CF₃ — Et racemic IV-1305 Me Me Me — CF₃ — Et (R)- IV-1306 Me Me Me — CF₃ — nPr racemic IV-1307 Me Me Me — CF₃ — nPr (R)- IV-1308 Me Me Me — CF₃ — iPr racemic IV-1309 Me Me Me — CF₃ — iPr (R)- IV-1310 Me Me Me — CF₃ — cPr racemic IV-1311 Me Me Me — CF₃ — cPr (R)- IV-1312 Me Me Me — CF₃ — Ph racemic IV-1313 Me Me Me — CF₃ — Ph (R)- IV-1314 Me Me Me — CH₂OH — H racemic IV-1315 Me Me Me — CH₂OH — H (R)- IV-1316 Me Me Me — CH₂OH — Me racemic IV-1317 Me Me Me — CH₂OH — Me (R)- IV-1318 Me Me Me — CH₂OH — CHF₂ racemic IV-1319 Me Me Me — CH₂OH — CHF₂ (R)- IV-1320 Me Me Me — CH₂OH — CF₃ racemic IV-1321 Me Me Me — CH₂OH — CF₃ (R)- IV-1322 Me Me Me — CH₂OH — Et racemic IV-1323 Me Me Me — CH₂OH — Et (R)- IV-1324 Me Me Me — CH₂OH — nPr racemic IV-1325 Me Me Me — CH₂OH — nPr (R)- IV-1326 Me Me Me — CH₂OH — iPr racemic IV-1327 Me Me Me — CH₂OH — iPr (R)- IV-1328 Me Me Me — CH₂OH — cPr racemic IV-1329 Me Me Me — CH₂OH — cPr (R)- IV-1330 Me Me Me — CH₂OH — Ph racemic IV-1331 Me Me Me — CH₂OH — Ph (R)- IV-1332 Me Me Me — CH₂OMe — H racemic IV-1333 Me Me Me — CH₂OMe — H (R)- IV-1334 Me Me Me — CH₂OMe — Me racemic IV-1335 Me Me Me — CH₂OMe — Me (R)- IV-1336 Me Me Me — CH₂OMe — CHF₂ racemic IV-1337 Me Me Me — CH₂OMe — CHF₂ (R)- IV-1338 Me Me Me — CH₂OMe — CF₃ racemic IV-1339 Me Me Me — CH₂OMe — CF₃ (R)- IV-1340 Me Me Me — CH₂OMe — Et racemic IV-1341 Me Me Me — CH₂OMe — Et (R)- IV-1342 Me Me Me — CH₂OMe — nPr racemic IV-1343 Me Me Me — CH₂OMe — nPr (R)- IV-1344 Me Me Me — CH₂OMe — iPr racemic IV-1345 Me Me Me — CH₂OMe — iPr (R)- IV-1346 Me Me Me — CH₂OMe — cPr racemic IV-1347 Me Me Me — CH₂OMe — cPr (R)- IV-1348 Me Me Me — CH₂OMe — Ph racemic IV-1349 Me Me Me — CH₂OMe — Ph (R)- IV-1350 Me Me Me — CH₂OBn — H racemic IV-1351 Me Me Me — CH₂OBn — H (R)-

TABLE 91 (IV)

Com- pound Config- No. R¹ R² R³ L² R⁴ L³ R⁵ uration IV-1352 Me Me Me — CH₂OBn — Me racemic IV-1353 Me Me Me — CH₂OBn — Me (R)- IV-1354 Me Me Me — CH₂OBn — Ph racemic IV-1355 Me Me Me — CH₂OBn — Ph (R)- IV-1356 Me Me Me — CH₂NMe₂ — H racemic IV-1357 Me Me Me — CH₂NMe₂ — H (R)- IV-1358 Me Me Me — CH₂NMe₂ — Me racemic IV-1359 Me Me Me — CH₂NMe₂ — Me (R)- IV-1360 Me Me Me — CH₂NMe₂ — CHF₂ racemic IV-1361 Me Me Me — CH₂NMe₂ — CHF₂ (R)- IV-1362 Me Me Me — CH₂NMe₂ — CF₃ racemic IV-1363 Me Me Me — CH₂NMe₂ — CF₃ (R)- IV-1364 Me Me Me — CH₂NMe₂ — Et racemic IV-1365 Me Me Me — CH₂NMe₂ — Et (R)- IV-1366 Me Me Me — CH₂NMe₂ — nPr racemic IV-1367 Me Me Me — CH₂NMe₂ — nPr (R)- IV-1368 Me Me Me — CH₂NMe₂ — iPr racemic IV-1369 Me Me Me — CH₂NMe₂ — iPr (R)- IV-1370 Me Me Me — CH₂NMe₂ — cPr racemic IV-1371 Me Me Me — CH₂NMe₂ — cPr (R)- IV-1372 Me Me Me — CH₂NMe₂ — Ph racemic IV-1373 Me Me Me — CH₂NMe₂ — Ph (R)- IV-1374 Me Me Me — CH₂-3-(3,3-(3, — H racemic — pyrrolidyl) — IV-1375 Me Me Me — CH₂-3-(3,3-(3, — H (R)- — pyrrolidyl) — IV-1376 Me Me Me — CH₂-3-(3,3-(3, — Me racemic — pyrrolidyl) — IV-1377 Me Me Me — CH₂-3-(3,3-(3, — Me (R)- — pyrrolidyl) — IV-1378 Me Me Me — CH₂-3-(3,3-(3, — Ph racemic — pyrrolidyl) — IV-1379 Me Me Me — CH₂-3-(3,3-(3, — Ph (R)- — pyrrolidyl) — IV-1380 Me Me Me — 2-F—Ph — H racemic IV-1381 Me Me Me — 2-F—Ph — H (R)- IV-1382 Me Me Me — 2-F—Ph — Me racemic IV-1383 Me Me Me — 2-F—Ph — Me (R)- IV-1384 Me Me Me — 2-F—Ph — Me (S)- IV-1385 Me Me Me — 2-F—Ph — CHF₂ racemic IV-1386 Me Me Me — 2-F—Ph — CHF₂ (R)- IV-1387 Me Me Me — 2-F—Ph — CHF₂ (S)- IV-1388 Me Me Me — 2-F—Ph — CF₃ racemic IV-1389 Me Me Me — 2-F—Ph — CF₃ (R)- IV-1390 Me Me Me — 2-F—Ph — CF₃ (S)- IV-1391 Me Me Me — 2-F—Ph — Et racemic IV-1392 Me Me Me — 2-F—Ph — Et (R)- IV-1393 Me Me Me — 2-F—Ph — Et (S)- IV-1394 Me Me Me — 2-F—Ph — nPr racemic IV-1395 Me Me Me — 2-F—Ph — nPr (R)- IV-1396 Me Me Me — 2-F—Ph — iPr racemic IV-1397 Me Me Me — 2-F—Ph — iPr (R)- IV-1398 Me Me Me — 2-F—Ph — iPr (S)- IV-1399 Me Me Me — 2-F—Ph — cPr racemic IV-1400 Me Me Me — 2-F—Ph — cPr (R)- IV-1401 Me Me Me — 2-F—Ph — cPr (S)-

TABLE 92

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration IV-1402 Me Me Me — 3-F—Ph — H racemic IV-1403 Me Me Me — 3-F—Ph — H (R)- IV-1404 Me Me Me — 3-F—Ph — Me racemic IV-1405 Me Me Me — 3-F—Ph — Me (R)- IV-1406 Me Me Me — 3-F—Ph — Me (S)- IV-1407 Me Me Me — 3-F—Ph — CHF₂ racemic IV-1408 Me Me Me — 3-F—Ph — CHF₂ (R)- IV-1409 Me Me Me — 3-F—Ph — CHF₂ (S)- IV-1410 Me Me Me — 3-F—Ph — CF₃ racemic IV-1411 Me Me Me — 3-F—Ph — CF₃ (R)- IV-1412 Me Me Me — 3-F—Ph — CF₃ (S)- IV-1413 Me Me Me — 3-F—Ph — Et racemic IV-1414 Me Me Me — 3-F—Ph — Et (R)- IV-1415 Me Me Me — 3-F—Ph — Et (S)- IV-1416 Me Me Me — 3-F—Ph — nPr racemic IV-1417 Me Me Me — 3-F—Ph — nPr (R)- IV-1418 Me Me Me — 3-F—Ph — nPr (S)- IV-1419 Me Me Me — 3-F—Ph — iPr racemic IV-1420 Me Me Me — 3-F—Ph — iPr (R)- IV-1421 Me Me Me — 3-F—Ph — iPr (S)- IV-1422 Me Me Me — 3-F—Ph — cPr racemic IV-1423 Me Me Me — 3-F—Ph — cPr (R)- IV-1424 Me Me Me — 3-F—Ph — cPr (S)- IV-1425 Me Me Me — 4-F—Ph — H racemic IV-1426 Me Me Me — 4-F—Ph — H (R)- IV-1427 Me Me Me — 4-F—Ph — Me racemic IV-1428 Me Me Me — 4-F—Ph — Me (R)- IV-1429 Me Me Me — 4-F—Ph — Me (S)- IV-1430 Me Me Me — 4-F—Ph — CHF₂ racemic IV-1431 Me Me Me — 4-F—Ph — CHF₂ (R)- IV-1432 Me Me Me — 4-F—Ph — CHF₂ (S)- IV-1433 Me Me Me — 4-F—Ph — CF₃ racemic IV-1434 Me Me Me — 4-F—Ph — CF₃ (R)- IV-1435 Me Me Me — 4-F—Ph — CF₃ (S)- IV-1436 Me Me Me — 4-F—Ph — Et racemic IV-1437 Me Me Me — 4-F—Ph — Et (R)- IV-1438 Me Me Me — 4-F—Ph — Et (S)- IV-1439 Me Me Me — 4-F—Ph — nPr racemic IV-1440 Me Me Me — 4-F—Ph — nPr (R)- IV-1441 Me Me Me — 4-F—Ph — nPr (S)- IV-1442 Me Me Me — 4-F—Ph — iPr racemic IV-1443 Me Me Me — 4-F—Ph — iPr (R)- IV-1444 Me Me Me — 4-F—Ph — iPr (S)- IV-1445 Me Me Me — 4-F—Ph — cPr racemic IV-1446 Me Me Me — 4-F—Ph — cPr (R)- IV-1447 Me Me Me — 4-F—Ph — cPr (S)- IV-1448 Me Me Me — 2-Cl—Ph — H racemic IV-1449 Me Me Me — 2-Cl—Ph — H (R)- IV-1450 Me Me Me — 2-Cl—Ph — Me racemic IV-1451 Me Me Me — 2-Cl—Ph — Me (R)-

TABLE 93

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration IV-1452 Me Me Me — 2-Cl—Ph — CHF₂ racemic IV-1453 Me Me Me — 2-Cl—Ph — CHF₂ (R)- IV-1454 Me Me Me — 2-Cl—Ph — CF₃ racemic IV-1455 Me Me Me — 2-Cl—Ph — CF₃ (R)- IV-1456 Me Me Me — 2-Cl—Ph — Et racemic IV-1457 Me Me Me — 2-Cl—Ph — Et (R)- IV-1458 Me Me Me — 2-Cl—Ph — nPr racemic IV-1459 Me Me Me — 2-Cl—Ph — nPr (R)- IV-1460 Me Me Me — 2-Cl—Ph — iPr racemic IV-1461 Me Me Me — 2-Cl—Ph — iPr (R)- IV-1462 Me Me Me — 2-Cl—Ph — cPr racemic IV-1463 Me Me Me — 2-Cl—Ph — cPr (R)- IV-1464 Me Me Me — 3-Cl—Ph — H racemic IV-1465 Me Me Me — 3-Cl—Ph — H (R)- IV-1466 Me Me Me — 3-Cl—Ph — Me racemic IV-1467 Me Me Me — 3-Cl—Ph — Me (R)- IV-1468 Me Me Me — 3-Cl—Ph — CHF₂ racemic IV-1469 Me Me Me — 3-Cl—Ph — CHF₂ (R)- IV-1470 Me Me Me — 3-Cl—Ph — CF₃ racemic IV-1471 Me Me Me — 3-Cl—Ph — CF₃ (R)- IV-1472 Me Me Me — 3-Cl—Ph — Et racemic IV-1473 Me Me Me — 3-Cl—Ph — Et (R)- IV-1474 Me Me Me — 3-Cl—Ph — nPr racemic IV-1475 Me Me Me — 3-Cl—Ph — nPr (R)- IV-1476 Me Me Me — 3-Cl—Ph — iPr racemic IV-1477 Me Me Me — 3-Cl—Ph — iPr (R)- IV-1478 Me Me Me — 3-Cl—Ph — cPr racemic IV-1479 Me Me Me — 3-Cl—Ph — cPr (R)- IV-1480 Me Me Me — 4-Cl—Ph — H racemic IV-1481 Me Me Me — 4-Cl—Ph — H (R)- IV-1482 Me Me Me — 4-Cl—Ph — Me racemic IV-1483 Me Me Me — 4-Cl—Ph — Me (R)- IV-1484 Me Me Me — 4-Cl—Ph — CHF₂ racemic IV-1485 Me Me Me — 4-Cl—Ph — CHF₂ (R)- IV-1486 Me Me Me — 4-Cl—Ph — CF₃ racemic IV-1487 Me Me Me — 4-Cl—Ph — CF₃ (R)- IV-1488 Me Me Me — 4-Cl—Ph — Et racemic IV-1489 Me Me Me — 4-Cl—Ph — Et (R)- IV-1490 Me Me Me — 4-Cl—Ph — nPr racemic IV-1491 Me Me Me — 4-Cl—Ph — nPr (R)- IV-1492 Me Me Me — 4-Cl—Ph — iPr racemic IV-1493 Me Me Me — 4-Cl—Ph — iPr (R)- IV-1494 Me Me Me — 4-Cl—Ph — cPr racemic IV-1495 Me Me Me — 4-Cl—Ph — cPr (R)- IV-1496 Me Me Me — 2-Me—Ph — H racemic IV-1497 Me Me Me — 2-Me—Ph — H (R)- IV-1498 Me Me Me — 2-Me—Ph — Me racemic IV-1499 Me Me Me — 2-Me—Ph — Me (R)- IV-1500 Me Me Me — 2-Me—Ph — CHF₂ racemic IV-1501 Me Me Me — 2-Me—Ph — CHF₂ (R)-

TABLE 94

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration IV-1502 Me Me Me — 2-Me—Ph — CF₃ racemic IV-1503 Me Me Me — 2-Me—Ph — CF₃ (R)- IV-1504 Me Me Me — 2-Me—Ph — Et racemic IV-1505 Me Me Me — 2-Me—Ph — Et (R)- IV-1506 Me Me Me — 2-Me—Ph — nPr racemic IV-1507 Me Me Me — 2-Me—Ph — nPr (R)- IV-1508 Me Me Me — 2-Me—Ph — iPr racemic IV-1509 Me Me Me — 2-Me—Ph — iPr (R)- IV-1510 Me Me Me — 2-Me—Ph — cPr racemic IV-1511 Me Me Me — 2-Me—Ph — cPr (R)- IV-1512 Me Me Me — 3-Me—Ph — H racemic IV-1513 Me Me Me — 3-Me—Ph — H (R)- IV-1514 Me Me Me — 3-Me—Ph — Me racemic IV-1515 Me Me Me — 3-Me—Ph — Me (R)- IV-1516 Me Me Me — 3-Me—Ph — CHF₂ racemic IV-1517 Me Me Me — 3-Me—Ph — CHF₂ (R)- IV-1518 Me Me Me — 3-Me—Ph — CF₃ racemic IV-1519 Me Me Me — 3-Me—Ph — CF₃ (R)- IV-1520 Me Me Me — 3-Me—Ph — Et racemic IV-1521 Me Me Me — 3-Me—Ph — Et (R)- IV-1522 Me Me Me — 3-Me—Ph — nPr racemic IV-1523 Me Me Me — 3-Me—Ph — nPr (R)- IV-1524 Me Me Me — 3-Me—Ph — iPr racemic IV-1525 Me Me Me — 3-Me—Ph — iPr (R)- IV-1526 Me Me Me — 3-Me—Ph — cPr racemic IV-1527 Me Me Me — 3-Me—Ph — cPr (R)- IV-1528 Me Me Me — 4-Me—Ph — H racemic IV-1529 Me Me Me — 4-Me—Ph — H (R)- IV-1530 Me Me Me — 4-Me—Ph — Me racemic IV-1531 Me Me Me — 4-Me—Ph — Me (R)- IV-1532 Me Me Me — 4-Me—Ph — CHF₂ racemic IV-1533 Me Me Me — 4-Me—Ph — CHF₂ (R)- IV-1534 Me Me Me — 4-Me—Ph — CF₃ racemic IV-1535 Me Me Me — 4-Me—Ph — CF₃ (R)- IV-1536 Me Me Me — 4-Me—Ph — Et racemic IV-1537 Me Me Me — 4-Me—Ph — Et (R)- IV-1538 Me Me Me — 4-Me—Ph — nPr racemic IV-1539 Me Me Me — 4-Me—Ph — nPr (R)- IV-1540 Me Me Me — 4-Me—Ph — iPr racemic IV-1541 Me Me Me — 4-Me—Ph — iPr (R)- IV-1542 Me Me Me — 4-Me—Ph — cPr racemic IV-1543 Me Me Me — 4-Me—Ph — cPr (R)- IV-1544 Me Me Me — 2-thienyl — H racemic IV-1545 Me Me Me — 2-thienyl — H (S)- IV-1546 Me Me Me — 2-thienyl — Me racemic IV-1547 Me Me Me — 2-thienyl — Me (+)- IV-1548 Me Me Me — 2-thienyl — Me (−)- IV-1549 Me Me Me — 2-thienyl — CHF₂ racemic IV-1550 Me Me Me — 2-thienyl — CHF₂ (+)- IV-1551 Me Me Me — 2-thienyl — CHF₂ (−)-

TABLE 95

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration IV-1552 Me Me Me — 2-thienyl — CF₃ racemic IV-1553 Me Me Me — 2-thienyl — CF₃ (+)- IV-1554 Me Me Me — 2-thienyl — CF₃ (−)- IV-1555 Me Me Me — 2-thienyl — Et racemic IV-1556 Me Me Me — 2-thienyl — Et (+)- IV-1557 Me Me Me — 2-thienyl — Et (−)- IV-1558 Me Me Me — 2-thienyl — nPr racemic IV-1559 Me Me Me — 2-thienyl — nPr (+)- IV-1560 Me Me Me — 2-thienyl — nPr (−)- IV-1561 Me Me Me — 2-thienyl — iPr racemic IV-1562 Me Me Me — 2-thienyl — iPr (+)- IV-1563 Me Me Me — 2-thienyl — iPr (−)- IV-1564 Me Me Me — 2-thienyl — cPr racemic IV-1565 Me Me Me — 2-thienyl — cPr (+)- IV-1566 Me Me Me — 2-thienyl — cPr (−)- IV-1567 Me Me Me — 3-F-2-thienyl — H racemic IV-1568 Me Me Me — 3-F-2-thienyl — H (S)- IV-1569 Me Me Me — 3-F-2-thienyl — Me racemic IV-1570 Me Me Me — 3-F-2-thienyl — Me (S)- IV-1571 Me Me Me — 3-F-2-thienyl — CHF₂ racemic IV-1572 Me Me Me — 3-F-2-thienyl — CHF₂ (S)- IV-1573 Me Me Me — 3-F-2-thienyl — CF₃ racemic IV-1574 Me Me Me — 3-F-2-thienyl — CF₃ (S)- IV-1575 Me Me Me — 3-F-2-thienyl — Et racemic IV-1576 Me Me Me — 3-F-2-thienyl — Et (S)- IV-1577 Me Me Me — 3-F-2-thienyl — nPr racemic IV-1578 Me Me Me — 3-F-2-thienyl — nPr (S)- IV-1579 Me Me Me — 3-F-2-thienyl — iPr racemic IV-1580 Me Me Me — 3-F-2-thienyl — iPr (S)- IV-1581 Me Me Me — 3-F-2-thienyl — cPr racemic IV-1582 Me Me Me — 3-F-2-thienyl — cPr (S)- IV-1583 Me Me Me — 4-F-2-thienyl — H racemic IV-1584 Me Me Me — 4-F-2-thienyl — H (S)- IV-1585 Me Me Me — 4-F-2-thienyl — Me racemic IV-1586 Me Me Me — 4-F-2-thienyl — Me (S)- IV-1587 Me Me Me — 4-F-2-thienyl — CHF₂ racemic IV-1588 Me Me Me — 4-F-2-thienyl — CHF₂ (S)- IV-1589 Me Me Me — 4-F-2-thienyl — CF₃ racemic IV-1590 Me Me Me — 4-F-2-thienyl — CF₃ (S)- IV-1591 Me Me Me — 4-F-2-thienyl — Et racemic IV-1592 Me Me Me — 4-F-2-thienyl — Et (S)- IV-1593 Me Me Me — 4-F-2-thienyl — nPr racemic IV-1594 Me Me Me — 4-F-2-thienyl — nPr (S)- IV-1595 Me Me Me — 4-F-2-thienyl — iPr racemic IV-1596 Me Me Me — 4-F-2-thienyl — iPr (S)- IV-1597 Me Me Me — 4-F-2-thienyl — cPr racemic IV-1598 Me Me Me — 4-F-2-thienyl — cPr (S)- IV-1599 Me Me Me — 4-F-2-thienyl — H racemic IV-1600 Me Me Me — 4-F-2-thienyl — H (S)- IV-1601 Me Me Me — 4-F-2-thienyl — Me racemic

TABLE 96

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration IV-1602 Me Me Me — 5-F-2-thienyl — Me (S)- IV-1603 Me Me Me — 5-F-2-thienyl — CHF₂ racemic IV-1604 Me Me Me — 5-F-2-thienyl — CHF₂ (S)- IV-1605 Me Me Me — 5-F-2-thienyl — CF₃ racemic IV-1606 Me Me Me — 5-F-2-thienyl — CF₃ (S)- IV-1607 Me Me Me — 5-F-2-thienyl — Et racemic IV-1608 Me Me Me — 5-F-2-thienyl — Et (S)- IV-1609 Me Me Me — 5-F-2-thienyl — nPr racemic IV-1610 Me Me Me — 5-F-2-thienyl — nPr (S)- IV-1611 Me Me Me — 5-F-2-thienyl — iPr racemic IV-1612 Me Me Me — 5-F-2-thienyl — iPr (S)- IV-1613 Me Me Me — 5-F-2-thienyl — cPr racemic IV-1614 Me Me Me — 5-F-2-thienyl — cPr (S)- IV-1615 Me Me Me — 3-Cl-2-thienyl — H racemic IV-1616 Me Me Me — 3-Cl-2-thienyl — H (S)- IV-1617 Me Me Me — 3-Cl-2-thienyl — Me racemic IV-1618 Me Me Me — 3-Cl-2-thienyl — Me (S)- IV-1619 Me Me Me — 3-Cl-2-thienyl — CHF₂ racemic IV-1620 Me Me Me — 3-Cl-2-thienyl — CHF₂ (S)- IV-1621 Me Me Me — 3-Cl-2-thienyl — CF₃ racemic IV-1622 Me Me Me — 3-Cl-2-thienyl — CF₃ (S)- IV-1623 Me Me Me — 3-Cl-2-thienyl — Et racemic IV-1624 Me Me Me — 3-Cl-2-thienyl — Et (S)- IV-1625 Me Me Me — 3-Cl-2-thienyl — nPr racemic IV-1626 Me Me Me — 3-Cl-2-thienyl — nPr (S)- IV-1627 Me Me Me — 3-Cl-2-thienyl — iPr racemic IV-1628 Me Me Me — 3-Cl-2-thienyl — iPr (S)- IV-1629 Me Me Me — 3-Cl-2-thienyl — cPr racemic IV-1630 Me Me Me — 3-Cl-2-thienyl — cPr (S)- IV-1631 Me Me Me — 4-Cl-2-thienyl — H racemic IV-1632 Me Me Me — 4-Cl-2-thienyl — H (S)- IV-1633 Me Me Me — 4-Cl-2-thienyl — Me racemic IV-1634 Me Me Me — 4-Cl-2-thienyl — Me (S)- IV-1635 Me Me Me — 4-Cl-2-thienyl — CHF₂ racemic IV-1636 Me Me Me — 4-Cl-2-thienyl — CHF₂ (S)- IV-1637 Me Me Me — 4-Cl-2-thienyl — CF₃ racemic IV-1638 Me Me Me — 4-Cl-2-thienyl — CF₃ (S)- IV-1639 Me Me Me — 4-Cl-2-thienyl — Et racemic IV-1640 Me Me Me — 4-Cl-2-thienyl — Et (S)- IV-1641 Me Me Me — 4-Cl-2-thienyl — nPr racemic IV-1642 Me Me Me — 4-Cl-2-thienyl — nPr (S)- IV-1643 Me Me Me — 4-Cl-2-thienyl — iPr racemic IV-1644 Me Me Me — 4-Cl-2-thienyl — iPr (S)- IV-1645 Me Me Me — 4-Cl-2-thienyl — cPr racemic IV-1646 Me Me Me — 4-Cl-2-thienyl — cPr (S)- IV-1647 Me Me Me — 5-Cl-2-thienyl — H racemic IV-1648 Me Me Me — 5-Cl-2-thienyl — H (S)- IV-1649 Me Me Me — 5-Cl-2-thienyl — Me racemic IV-1650 Me Me Me — 5-Cl-2-thienyl — Me (S)- IV-1651 Me Me Me — 5-Cl-2-thienyl — CHF₂ racemic

TABLE 97

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration IV-1652 Me Me Me — 5-Cl-2-thienyl — CHF₂ (S)- IV-1653 Me Me Me — 5-Cl-2-thienyl — CF₃ racemic IV-1654 Me Me Me — 5-Cl-2-thienyl — CF₃ (S)- IV-1655 Me Me Me — 5-Cl-2-thienyl — Et racemic IV-1656 Me Me Me — 5-Cl-2-thienyl — Et (S)- IV-1657 Me Me Me — 5-Cl-2-thienyl — nPr racemic IV-1658 Me Me Me — 5-Cl-2-thienyl — nPr (S)- IV-1659 Me Me Me — 5-Cl-2-thienyl — iPr racemic IV-1660 Me Me Me — 5-Cl-2-thienyl — iPr (S)- IV-1661 Me Me Me — 5-Cl-2-thienyl — cPr racemic IV-1662 Me Me Me — 5-Cl-2-thienyl — cPr (S)- IV-1663 Me Me Me — 3-Me-2-thienyl — H racemic IV-1664 Me Me Me — 3-Me-2-thienyl — H (S)- IV-1665 Me Me Me — 3-Me-2-thienyl — Me racemic IV-1666 Me Me Me — 3-Me-2-thienyl — Me (S)- IV-1667 Me Me Me — 3-Me-2-thienyl — CHF₂ racemic IV-1668 Me Me Me — 3-Me-2-thienyl — CHF₂ (S)- IV-1669 Me Me Me — 3-Me-2-thienyl — CF₃ racemic IV-1670 Me Me Me — 3-Me-2-thienyl — CF₃ (S)- IV-1671 Me Me Me — 3-Me-2-thienyl — Et racemic IV-1672 Me Me Me — 3-Me-2-thienyl — Et (S)- IV-1673 Me Me Me — 3-Me-2-thienyl — nPr racemic IV-1674 Me Me Me — 3-Me-2-thienyl — nPr (S)- IV-1675 Me Me Me — 3-Me-2-thienyl — iPr racemic IV-1676 Me Me Me — 3-Me-2-thienyl — iPr (S)- IV-1677 Me Me Me — 3-Me-2-thienyl — cPr racemic IV-1678 Me Me Me — 3-Me-2-thienyl — cPr (S)- IV-1679 Me Me Me — 4-Me-2-thienyl — H racemic IV-1680 Me Me Me — 4-Me-2-thienyl — H (S)- IV-1681 Me Me Me — 4-Me-2-thienyl — Me racemic IV-1682 Me Me Me — 4-Me-2-thienyl — Me (S)- IV-1683 Me Me Me — 4-Me-2-thienyl — CHF₂ racemic IV-1684 Me Me Me — 4-Me-2-thienyl — CHF₂ (S)- IV-1685 Me Me Me — 4-Me-2-thienyl — CF₃ racemic IV-1686 Me Me Me — 4-Me-2-thienyl — CF₃ (S)- IV-1687 Me Me Me — 4-Me-2-thienyl — Et racemic IV-1688 Me Me Me — 4-Me-2-thienyl — Et (S)- IV-1689 Me Me Me — 4-Me-2-thienyl — nPr racemic IV-1690 Me Me Me — 4-Me-2-thienyl — nPr (S)- IV-1691 Me Me Me — 4-Me-2-thienyl — iPr racemic IV-1692 Me Me Me — 4-Me-2-thienyl — iPr (S)- IV-1693 Me Me Me — 4-Me-2-thienyl — cPr racemic IV-1694 Me Me Me — 4-Me-2-thienyl — cPr (S)- IV-1695 Me Me Me — 5-Me-2-thienyl — H racemic IV-1696 Me Me Me — 5-Me-2-thienyl — H (S)- IV-1697 Me Me Me — 5-Me-2-thienyl — Me racemic IV-1698 Me Me Me — 5-Me-2-thienyl — Me (S)- IV-1699 Me Me Me — 5-Me-2-thienyl — CHF₂ racemic IV-1700 Me Me Me — 5-Me-2-thienyl — CHF₂ (S)- IV-1701 Me Me Me — 5-Me-2-thienyl — CF₃ racemic

TABLE 98

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁵ figuration IV-1702 Me Me Me — 5-Me-2 -thienyl — CF₃ (S)- IV-1703 Me Me Me — 5-Me-2 -thienyl — Et racemic IV-1704 Me Me Me — 5-Me-2 -thienyl — Et (S)- IV-1705 Me Me Me — 5-Me-2 -thienyl — nPr racemic IV-1706 Me Me Me — 5-Me-2-thienyl — nPr (S)- IV-1707 Me Me Me — 5-Me-2 -thienyl — iPr racemic IV-1708 Me Me Me — 5-Me-2-thienyl — iPr (S)- IV-1709 Me Me Me — 5-Me-2-thienyl — cPr racemic IV-1710 Me Me Me — 5-Me-2-thienyl — cPr (S)- IV-1711 Me Me Me — 3-thienyl — H racemic IV-1712 Me Me Me — 3-thienyl — H (R)- IV-1713 Me Me Me — 3-thienyl — Me racemic IV-1714 Me Me Me — 3-thienyl — Me (R)- IV-1715 Me Me Me — 3-thienyl — CHF₂ racemic IV-1716 Me Me Me — 3-thienyl — CHF₂ (R) — IV-1717 Me Me Me — 3-thienyl — CF₃ racemic IV-1718 Me Me Me — 3-thienyl — CF₃ (R) — IV-1719 Me Me Me — 3-thienyl — Et racemic IV-1720 Me Me Me — 3-thienyl — Et (R)- IV-1721 Me Me Me — 3-thienyl — nPr racemic IV-1722 Me Me Me — 3-thienyl — nPr (R)- IV-1723 Me Me Me — 3-thienyl — iPr racemic IV-1724 Me Me Me — 3-thienyl — iPr (R)- IV-1725 Me Me Me — 3-thienyl — cPr racemic IV-1726 Me Me Me — 3-thienyl — cPr (R)-

TABLE 99

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁶ figuration V-1 Me Me Me O Ph CH₂ Me racemic V-2 Me Me Me O Ph CH₂ Me (S)- V-3 Me Et Me O Ph CH₂ Me racemic V-4 Me Et Me O Ph CH₂ Me (S)- V-5 Me Me Me O Ph CH₂ Et racemic V-6 Me Me Me O Ph CH₂ Et (S)- V-7 Me Et Me O Ph CH₂ Et racemic V-8 Me Et Me O Ph CH₂ Et (S)- V-9 Me Me Me O Ph CH₂ nPr racemic V-10 Me Me Me O Ph CH₂ nPr (S)- V-11 Me Et Me O Ph CH₂ nPr racemic V-12 Me Et Me O Ph CH₂ nPr (S)- V-13 Me Me Me O Ph CH₂ iPr racemic V-14 Me Me Me O Ph CH₂ iPr (S)- V-15 Me Et Me O Ph CH₂ iPr racemic V-16 Me Et Me O Ph CH₂ iPr (S)- V-17 Me Me Me O Ph CH₂ nBu racemic V-18 Me Me Me O Ph CH₂ nBu (S)- V-19 Me Et Me O Ph CH₂ nBu racemic V-20 Me Et Me O Ph CH₂ nBu (S)- V-21 Me Me Me O Ph CH₂ tBu racemic V-22 Me Me Me O Ph CH₂ tBu (S)- V-23 Me Et Me O Ph CH₂ tBu racemic V-24 Me Et Me O Ph CH₂ tBu (S)- V-25 Me Me Me O Ph CH₂ iBu racemic V-26 Me Me Me O Ph CH₂ iBu (S)- V-27 Me Et Me O Ph CH₂ iBu racemic V-28 Me Et Me O Ph CH₂ iBu (S)- V-29 Me Me Me O Ph CH₂ n-Heptyl racemic V-30 Me Me Me O Ph CH₂ n-Heptyl (S)- V-31 Me Et Me O Ph CH₂ n-Heptyl racemic V-32 Me Et Me O Ph CH₂ n-Heptyl (S)- V-33 Me Me Me O Ph CH₂ n-Undecyl racemic V-34 Me Me Me O Ph CH₂ n-Undecyl (S)- V-35 Me Et Me O Ph CH₂ n-Undecyl racemic V-36 Me Et Me O Ph CH₂ n-Undecyl (S)- V-37 Me Me Me O Ph CH₂ Ph racemic V-38 Me Me Me O Ph CH₂ Ph (S)- V-39 Me Et Me O Ph CH₂ Ph racemic V-40 Me Et Me O Ph CH₂ Ph (S)- V-41 Me Me Me O Ph CH₂ OEt racemic V-42 Me Me Me O Ph CH₂ OEt (S)- V-43 Me Et Me O Ph CH₂ OEt racemic V-44 Me Et Me O Ph CH₂ OEt (S)- V-45 Me Me Me O Ph CH₂ (CH₂)₂COOH racemic V-46 Me Me Me O Ph CH₂ (CH₂)₂COOH (S)- V-47 Me Et Me O Ph CH₂ (CH₂)₂COOH racemic V-48 Me Et Me O Ph CH₂ (CH₂)₂COOH (S)- V-49 Me Me Me O Ph C(Me)₂ Me racemic V-50 Me Me Me O Ph C(Me)₂ Me (S)-

TABLE 100

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁶ figuration V-51 Me Et Me O Ph C(Me)₂ Me racemic V-52 Me Et Me O Ph C(Me)₂ Me (S)- V-53 Me Me Me O Ph C(Me)₂ Et racemic V-54 Me Me Me O Ph C(Me)₂ Et (S)- V-55 Me Et Me O Ph C(Me)₂ Et racemic V-56 Me Et Me O Ph C(Me)₂ Et (S)- V-57 Me Me Me O Ph C(Me)₂ nPr racemic V-58 Me Me Me O Ph C(Me)₂ nPr (S)- V-59 Me Et Me O Ph C(Me)₂ nPr racemic V-60 Me Et Me O Ph C(Me)₂ nPr (S)- V-61 Me Me Me O Ph C(Me)₂ iPr racemic V-62 Me Me Me O Ph C(Me)₂ iPr (S)- V-63 Me Et Me O Ph C(Me)₂ iPr racemic V-64 Me Et Me O Ph C(Me)₂ iPr (S)- V-65 Me Me Me O Ph C(Me)₂ nBu racemic V-66 Me Me Me O Ph C(Me)₂ nBu (S)- V-67 Me Et Me O Ph C(Me)₂ nBu racemic V-68 Me Et Me O Ph C(Me)₂ nBu (S)- V-69 Me Me Me O Ph C(Me)₂ tBu racemic V-70 Me Me Me O Ph C(Me)₂ tBu (S)- V-71 Me Et Me O Ph C(Me)₂ tBu racemic V-72 Me Et Me O Ph C(Me)₂ tBu (S)- V-73 Me Me Me O Ph C(Me)₂ iBu racemic V-74 Me Me Me O Ph C(Me)₂ iBu (S)- V-75 Me Et Me O Ph C(Me)₂ iBu racemic V-76 Me Et Me O Ph C(Me)₂ iBu (S)- V-77 Me Me Me O Ph C(Me)₂ n-Heptyl racemic V-78 Me Me Me O Ph C(Me)₂ n-Heptyl (S)- V-79 Me Et Me O Ph C(Me)₂ n-Heptyl racemic V-80 Me Et Me O Ph C(Me)₂ n-Heptyl (S)- V-81 Me Me Me O Ph C(Me)₂ n-Undecyl racemic V-82 Me Me Me O Ph C(Me)₂ n-Undecyl (S)- V-83 Me Et Me O Ph C(Me)₂ n-Undecyl racemic V-84 Me Et Me O Ph C(Me)₂ n-Undecyl (S)- V-85 Me Me Me O Ph C(Me)₂ Ph racemic V-86 Me Me Me O Ph C(Me)₂ Ph (S)- V-87 Me Et Me O Ph C(Me)₂ Ph racemic V-88 Me Et Me O Ph C(Me)₂ Ph (S)- V-89 Me Me Me O Ph C(Me)₂ OEt racemic V-90 Me Me Me O Ph C(Me)₂ OEt (S)- V-91 Me Et Me O Ph C(Me)₂ OEt racemic V-92 Me Et Me O Ph C(Me)₂ OEt (S)- V-93 Me Me Me O Ph C(Me)₂ (CH₂)₂COOH racemic V-94 Me Me Me O Ph C(Me)₂ (CH₂)₂COOH (S)- V-95 Me Et Me O Ph C(Me)₂ (CH₂)₂COOH racemic V-96 Me Et Me O Ph C(Me)₂ (CH₂)₂COOH (S)- V-97 Me Me Me O Ph (CH₂)₂ Me racemic V-98 Me Me Me O Ph (CH₂)₂ Me (R)- V-99 Me Et Me O Ph (CH₂)₂ Me racemic V-100 Me Et Me O Ph (CH₂)₂ Me (R)-

TABLE 101

Compound Config- No. R¹ R² R³ L² R⁴ L³ R⁶ uration V-101 Me Me Me O Ph (CH₂)₂ Et racemic V-102 Me Me Me O Ph (CH₂)₂ Et (R)- V-103 Me Et Me O Ph (CH₂)₂ Et racemic V-104 Me Et Me O Ph (CH₂)₂ Et (R)- V-105 Me Me Me O Ph (CH₂)₂ nPr racemic V-106 Me Me Me O Ph (CH₂)₂ nPr (R)- V-107 Me Et Me O Ph (CH₂)₂ nPr racemic V-108 Me Et Me O Ph (CH₂)₂ nPr (R)- V-109 Me Me Me O Ph (CH₂)₂ iPr racemic V-110 Me Me Me O Ph (CH₂)₂ iPr (R)- V-111 Me Et Me O Ph (CH₂)₂ iPr racemic V-112 Me Et Me O Ph (CH₂)₂ iPr (R)- V-113 Me Me Me O Ph (CH₂)₂ nBu racemic V-114 Me Me Me O Ph (CH₂)₂ nBu (R)- V-115 Me Et Me O Ph (CH₂)₂ nBu racemic V-116 Me Et Me O Ph (CH₂)₂ nBu (R)- V-117 Me Me Me O Ph (CH₂)₂ tBu racemic V-118 Me Me Me O Ph (CH₂)₂ tBu (R)- V-119 Me Et Me O Ph (CH₂)₂ tBu racemic V-120 Me Et Me O Ph (CH₂)₂ tBu (R)- V-121 Me Me Me O Ph (CH₂)₂ iBu racemic V-122 Me Me Me O Ph (CH₂)₂ iBu (R)- V-123 Me Et Me O Ph (CH₂)₂ iBu racemic V-124 Me Et Me O Ph (CH₂)₂ iBu (R)- V-125 Me Me Me O Ph (CH₂)₂ n-Heptyl racemic V-126 Me Me Me O Ph (CH₂)₂ n-Heptyl (R)- V-127 Me Et Me O Ph (CH₂)₂ n-Heptyl racemic V-128 Me Et Me O Ph (CH₂)₂ n-Heptyl (R)- V-129 Me Me Me O Ph (CH₂)₂ n-Undecyl racemic V-130 Me Me Me O Ph (CH₂)₂ n-Undecyl (R)- V-131 Me Et Me O Ph (CH₂)₂ n-Undecyl racemic V-132 Me Et Me O Ph (CH₂)₂ n-Undecyl (R)- V-133 Me Me Me O Ph (CH₂)₂ Ph racemic V-134 Me Me Me O Ph (CH₂)₂ Ph (R)- V-135 Me Et Me O Ph (CH₂)₂ Ph racemic V-136 Me Et Me O Ph (CH₂)₂ Ph (R)- V-137 Me Me Me O Ph (CH₂)₂ OEt racemic V-138 Me Me Me O Ph (CH₂)₂ OEt (R)- V-139 Me Et Me O Ph (CH₂)₂ OEt racemic V-140 Me Et Me O Ph (CH₂)₂ OEt (R)- V-141 Me Me Me O Ph (CH₂)₂ (CH₂)₂COOH racemic V-142 Me Me Me O Ph (CH₂)₂ (CH₂)₂COOH (R)- V-143 Me Et Me O Ph (CH₂)₂ (CH₂)₂COOH racemic V-144 Me Et Me O Ph (CH₂)₂ (CH₂)₂COOH (R)- V-145 Me Me Me O Ph CH₂C(Me)₂ Me racemic V-146 Me Me Me O Ph CH₂C(Me)₂ Me (R)- V-147 Me Et Me O Ph CH₂C(Me)₂ Me racemic V-148 Me Et Me O Ph CH₂C(Me)₂ Me (R)- V-149 Me Me Me O Ph CH₂C(Me)₂ Et racemic V-150 Me Me Me O Ph CH₂C(Me)₂ Et (R)-

TABLE 102 (Va)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-151 Me Et Me O Ph CH₂C(Me)₂ Et racemic V-152 Me Et Me O Ph CH₂C(Me)₂ Et (R)- V-153 Me Me Me O Ph CH₂C(Me)₂ nPr racemic V-154 Me Me Me O Ph CH₂C(Me)₂ nPr (R)- V-155 Me Et Me O Ph CH₂C(Me)₂ nPr racemic V-156 Me Et Me O Ph CH₂C(Me)₂ nPr (R)- V-157 Me Me Me O Ph CH₂C(Me)₂ iPr racemic V-158 Me Me Me O Ph CH₂C(Me)₂ iPr (R)- V-159 Me Et Me O Ph CH₂C(Me)₂ iPr racemic V-160 Me Et Me O Ph CH₂C(Me)₂ iPr (R)- V-161 Me Me Me O Ph CH₂C(Me)₂ nBu racemic V-162 Me Me Me O Ph CH₂C(Me)₂ nBu (R)- V-163 Me Et Me O Ph CH₂C(Me)₂ nBu racemic V-164 Me Et Me O Ph CH₂C(Me)₂ nBu (R)- V-165 Me Me Me O Ph CH₂C(Me)₂ tBu racemic V-166 Me Me Me O Ph CH₂C(Me)₂ tBu (R)- V-167 Me Et Me O Ph CH₂C(Me)₂ tBu racemic V-168 Me Et Me O Ph CH₂C(Me)₂ tBu (R)- V-169 Me Me Me O Ph CH₂C(Me)₂ iBu racemic V-170 Me Me Me O Ph CH₂C(Me)₂ iBu (R)- V-171 Me Et Me O Ph CH₂C(Me)₂ iBu racemic V-172 Me Et Me O Ph CH₂C(Me)₂ iBu (R)- V-173 Me Me Me O Ph CH₂C(Me)₂ n-Heptyl racemic V-174 Me Me Me O Ph CH₂C(Me)₂ n-Heptyl (R)- V-175 Me Et Me O Ph CH₂C(Me)₂ n-Heptyl racemic V-176 Me Et Me O Ph CH₂C(Me)₂ n-Heptyl (R)- V-177 Me Me Me O Ph CH₂C(Me)₂ n-Undecyl racemic V-178 Me Me Me O Ph CH₂C(Me)₂ n-Undecyl (R)- V-179 Me Et Me O Ph CH₂C(Me)₂ n-Undecyl racemic V-180 Me Et Me O Ph CH₂C(Me)₂ n-Undecyl (R)- V-181 Me Me Me O Ph CH₂C(Me)₂ Ph racemic V-182 Me Me Me O Ph CH₂C(Me)₂ Ph (R)- V-183 Me Et Me O Ph CH₂C(Me)₂ Ph racemic V-184 Me Et Me O Ph CH₂C(Me)₂ Ph (R)- V-185 Me Me Me O Ph CH₂C(Me)₂ OEt racemic V-186 Me Me Me O Ph CH₂C(Me)₂ OEt (R)- V-187 Me Et Me O Ph CH₂C(Me)₂ OEt racemic V-188 Me Et Me O Ph CH₂C(Me)₂ OEt (R)- V-189 Me Me Me O Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-190 Me Me Me O Ph CH₂C(Me)₂ (CH₂)₂COOH (R)- V-191 Me Et Me O Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-192 Me Et Me O Ph CH₂C(Me)₂ (CH₂)₂COOH (R)- V-193 Me Me Me NH Ph CH₂ Me racemic V-194 Me Me Me NH Ph CH₂ Me (S)- V-195 Me Et Me NH Ph CH₂ Me racemic V-196 Me Et Me NH Ph CH₂ Me (S)- V-197 Me Me Me NH Ph CH₂ Et racemic V-198 Me Me Me NH Ph CH₂ Et (S)- V-199 Me Et Me NH Ph CH₂ Et racemic V-200 Me Et Me NH Ph CH₂ Et (S)-

TABLE 103 (Va)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-201 Me Me Me NH Ph CH₂ nPr racemic V-202 Me Me Me NH Ph CH₂ nPr (S)- V-203 Me Et Me NH Ph CH₂ nPr racemic V-204 Me Et Me NH Ph CH₂ nPr (S)- V-205 Me Me Me NH Ph CH₂ iPr racemic V-206 Me Me Me NH Ph CH₂ iPr (S)- V-207 Me Et Me NH Ph CH₂ iPr racemic V-208 Me Et Me NH Ph CH₂ iPr (S)- V-209 Me Me Me NH Ph CH₂ nBu racemic V-210 Me Me Me NH Ph CH₂ nBu (S)- V-211 Me Et Me NH Ph CH₂ nBu racemic V-212 Me Et Me NH Ph CH₂ nBu (S)- V-213 Me Me Me NH Ph CH₂ tBu racemic V-214 Me Me Me NH Ph CH₂ tBu (S)- V-215 Me Et Me NH Ph CH₂ tBu racemic V-216 Me Et Me NH Ph CH₂ tBu (S)- V-217 Me Me Me NH Ph CH₂ iBu racemic V-218 Me Me Me NH Ph CH₂ iBu (S)- V-219 Me Et Me NH Ph CH₂ iBu racemic V-220 Me Et Me NH Ph CH₂ iBu (S)- V-221 Me Me Me NH Ph CH₂ n-Heptyl racemic V-222 Me Me Me NH Ph CH₂ n-Heptyl (S)- V-223 Me Et Me NH Ph CH₂ n-Heptyl racemic V-224 Me Et Me NH Ph CH₂ n-Heptyl (S)- V-225 Me Me Me NH Ph CH₂ n-Undecyl racemic V-226 Me Me Me NH Ph CH₂ n-Undecyl (S)- V-227 Me Et Me NH Ph CH₂ n-Undecyl racemic V-228 Me Et Me NH Ph CH₂ n-Undecyl (S)- V-229 Me Me Me NH Ph CH₂ Ph racemic V-230 Me Me Me NH Ph CH₂ Ph (S)- V-231 Me Et Me NH Ph CH₂ Ph racemic V-232 Me Et Me NH Ph CH₂ Ph (S)- V-233 Me Me Me NH Ph CH₂ OEt racemic V-234 Me Me Me NH Ph CH₂ OEt (S)- V-235 Me Et Me NH Ph CH₂ OEt racemic V-236 Me Et Me NH Ph CH₂ OEt (S)- V-237 Me Me Me NH Ph CH₂ (CH₂)₂COOH racemic V-238 Me Me Me NH Ph CH₂ (CH₂)₂COOH (S)- V-239 Me Et Me NH Ph CH₂ (CH₂)₂COOH racemic V-240 Me Et Me NH Ph CH₂ (CH₂)₂COOH (S)- V-241 Me Me Me NH Ph C(Me)₂ Me racemic V-242 Me Me Me NH Ph C(Me)₂ Me (S)- V-243 Me Et Me NH Ph C(Me)₂ Me racemic V-244 Me Et Me NH Ph C(Me)₂ Me (S)- V-245 Me Me Me NH Ph C(Me)₂ Et racemic V-246 Me Me Me NH Ph C(Me)₂ Et (S)- V-247 Me Et Me NH Ph C(Me)₂ Et racemic V-248 Me Et Me NH Ph C(Me)₂ Et (S)- V-249 Me Me Me NH Ph C(Me)₂ nPr racemic V-250 Me Me Me NH Ph C(Me)₂ nPr (S)-

TABLE 104 (Va)

Compound No. R¹ R² R³ L² R⁴ L³ R⁶ Configuration V-251 Me Et Me NH Ph C(Me)₂ nPr racemic V-252 Me Et Me NH Ph C(Me)₂ nPr (S)- V-253 Me Me Me NH Ph C(Me)₂ iPr racemic V-254 Me Me Me NH Ph C(Me)₂ iPr (S)- V-255 Me Et Me NH Ph C(Me)₂ iPr racemic V-256 Me Et Me NH Ph C(Me)₂ iPr (S)- V-257 Me Me Me NH Ph C(Me)₂ nBu racemic V-258 Me Me Me NH Ph C(Me)₂ nBu (S)- V-259 Me Et Me NH Ph C(Me)₂ nBu racemic V-260 Me Et Me NH Ph C(Me)₂ nBu (S)- V-261 Me Me Me NH Ph C(Me)₂ tBu racemic V-262 Me Me Me NH Ph C(Me)₂ tBu (S)- V-263 Me Et Me NH Ph C(Me)₂ tBu racemic V-264 Me Et Me NH Ph C(Me)₂ tBu (S)- V-265 Me Me Me NH Ph C(Me)₂ iBu racemic V-266 Me Me Me NH Ph C(Me)₂ iBu (S)- V-267 Me Et Me NH Ph C(Me)₂ iBu racemic V-268 Me Et Me NH Ph C(Me)₂ iBu (S)- V-269 Me Me Me NH Ph C(Me)₂ n-Heptyl racemic V-270 Me Me Me NH Ph C(Me)₂ n-Heptyl (S)- V-271 Me Et Me NH Ph C(Me)₂ n-Heptyl racemic V-272 Me Et Me NH Ph C(Me)₂ n-Heptyl (S)- V-273 Me Me Me NH Ph C(Me)₂ n-Undecyl racemic V-274 Me Me Me NH Ph C(Me)₂ n-Undecyl (S)- V-275 Me Et Me NH Ph C(Me)₂ n-Undecyl racemic V-276 Me Et Me NH Ph C(Me)₂ n-Undecyl (S)- V-277 Me Me Me NH Ph C(Me)₂ Ph racemic V-278 Me Me Me NH Ph C(Me)₂ Ph (S)- V-279 Me Et Me NH Ph C(Me)₂ Ph racemic V-280 Me Et Me NH Ph C(Me)₂ Ph (S)- V-281 Me Me Me NH Ph C(Me)₂ OEt racemic V-282 Me Me Me NH Ph C(Me)₂ OEt (S)- V-283 Me Et Me NH Ph C(Me)₂ OEt racemic V-284 Me Et Me NH Ph C(Me)₂ OEt (S)- V-285 Me Me Me NH Ph C(Me)₂ (CH₂)₂COOH racemic V-286 Me Me Me NH Ph C(Me)₂ (CH₂)₂COOH (S)- V-287 Me Et Me NH Ph C(Me)₂ (CH₂)₂COOH racemic V-288 Me Et Me NH Ph C(Me)₂ (CH₂)₂COOH (S)- V-289 Me Me Me NH Ph (CH₂)₂ Me racemic V-290 Me Me Me NH Ph (CH₂)₂ Me (R)- V-291 Me Et Me NH Ph (CH₂)₂ Me racemic V-292 Me Et Me NH Ph (CH₂)₂ Me (R)- V-293 Me Me Me NH Ph (CH₂)₂ Et racemic V-294 Me Me Me NH Ph (CH₂)₂ Et (R)- V-295 Me Et Me NH Ph (CH₂)₂ Et racemic V-296 Me Et Me NH Ph (CH₂)₂ Et (R)- V-297 Me Me Me NH Ph (CH₂)₂ nPr racemic V-298 Me Me Me NH Ph (CH₂)₂ nPr (R)- V-299 Me Et Me NH Ph (CH₂)₂ nPr racemic V-300 Me Et Me NH Ph (CH₂)₂ nPr (R)-

TABLE 105 (Va)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-301 Me Me Me NH Ph (CH₂)₂ iPr racemic V-302 Me Me Me NH Ph (CH₂)₂ iPr (R)- V-303 Me Et Me NH Ph (CH₂)₂ iPr racemic V-304 Me Et Me NH Ph (CH₂)₂ iPr (R)- V-305 Me Me Me NH Ph (CH₂)₂ nBu racemic V-306 Me Me Me NH Ph (CH₂)₂ nBu (R)- V-307 Me Et Me NH Ph (CH₂)₂ nBu racemic V-308 Me Et Me NH Ph (CH₂)₂ nBu (R)- V-309 Me Me Me NH Ph (CH₂)₂ tBu racemic V-310 Me Me Me NH Ph (CH₂)₂ tBu (R)- V-311 Me Et Me NH Ph (CH₂)₂ tBu racemic V-312 Me Et Me NH Ph (CH₂)₂ tBu (R)- V-313 Me Me Me NH Ph (CH₂)₂ iBu racemic V-314 Me Me Me NH Ph (CH₂)₂ iBu (R)- V-315 Me Et Me NH Ph (CH₂)₂ iBu racemic V-316 Me Et Me NH Ph (CH₂)₂ iBu (R)- V-317 Me Me Me NH Ph (CH₂)₂ n-Heptyl racemic V-318 Me Me Me NH Ph (CH₂)₂ n-Heptyl (R)- V-319 Me Et Me NH Ph (CH₂)₂ n-Heptyl racemic V-320 Me Et Me NH Ph (CH₂)₂ n-Heptyl (R)- V-321 Me Me Me NH Ph (CH₂)₂ n-Undecyl racemic V-322 Me Me Me NH Ph (CH₂)₂ n-Undecyl (R)- V-323 Me Et Me NH Ph (CH₂)₂ n-Undecyl racemic V-324 Me Et Me NH Ph (CH₂)₂ n-Undecyl (R)- V-325 Me Me Me NH Ph (CH₂)₂ Ph racemic V-326 Me Me Me NH Ph (CH₂)₂ Ph (R)- V-327 Me Et Me NH Ph (CH₂)₂ Ph racemic V-328 Me Et Me NH Ph (CH₂)₂ Ph (R)- V-329 Me Me Me NH Ph (CH₂)₂ OEt racemic V-330 Me Me Me NH Ph (CH₂)₂ OEt (R)- V-331 Me Et Me NH Ph (CH₂)₂ OEt racemic V-332 Me Et Me NH Ph (CH₂)₂ OEt (R)- V-333 Me Me Me NH Ph (CH₂)₂ (CH₂)₂COOH racemic V-334 Me Me Me NH Ph (CH₂)₂ (CH₂)₂COOH (R)- V-335 Me Et Me NH Ph (CH₂)₂ (CH₂)₂COOH racemic V-336 Me Et Me NH Ph (CH₂)₂ (CH₂)₂COOH (R)- V-337 Me Me Me NH Ph CH₂C(Me)₂ Me racemic V-338 Me Me Me NH Ph CH₂C(Me)₂ Me (R)- V-339 Me Et Me NH Ph CH₂C(Me)₂ Me racemic V-340 Me Et Me NH Ph CH₂C(Me)₂ Me (R)- V-341 Me Me Me NH Ph CH₂C(Me)₂ Et racemic V-342 Me Me Me NH Ph CH₂C(Me)₂ Et (R)- V-343 Me Et Me NH Ph CH₂C(Me)₂ Et racemic V-344 Me Et Me NH Ph CH₂C(Me)₂ Et (R)- V-345 Me Me Me NH Ph CH₂C(Me)₂ nPr racemic V-346 Me Me Me NH Ph CH₂C(Me)₂ nPr (R)- V-347 Me Et Me NH Ph CH₂C(Me)₂ nPr racemic V-348 Me Et Me NH Ph CH₂C(Me)₂ nPr (R)- V-349 Me Me Me NH Ph CH₂C(Me)₂ iPr racemic V-350 Me Me Me NH Ph CH₂C(Me)₂ iPr (R)-

TABLE 106 (Va)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-351 Me Et Me NH Ph CH₂C(Me)₂ iPr racemic V-352 Me Et Me NH Ph CH₂C(Me)₂ iPr (R)- V-353 Me Me Me NH Ph CH₂C(Me)₂ nBu racemic V-354 Me Me Me NH Ph CH₂C(Me)₂ nBu (R)- V-355 Me Et Me NH Ph CH₂C(Me)₂ nBu racemic V-356 Me Et Me NH Ph CH₂C(Me)₂ nBu (R)- V-357 Me Me Me NH Ph CH₂C(Me)₂ tBu racemic V-358 Me Me Me NH Ph CH₂C(Me)₂ tBu (R)- V-359 Me Et Me NH Ph CH₂C(Me)₂ tBu racemic V-360 Me Et Me NH Ph CH₂C(Me)₂ tBu (R)- V-361 Me Me Me NH Ph CH₂C(Me)₂ iBu racemic V-362 Me Me Me NH Ph CH₂C(Me)₂ iBu (R)- V-363 Me Et Me NH Ph CH₂C(Me)₂ iBu racemic V-364 Me Et Me NH Ph CH₂C(Me)₂ iBu (R)- V-365 Me Me Me NH Ph CH₂C(Me)₂ n-Heptyl racemic V-366 Me Me Me NH Ph CH₂C(Me)₂ n-Heptyl (R)- V-367 Me Et Me NH Ph CH₂C(Me)₂ n-Heptyl racemic V-368 Me Et Me NH Ph CH₂C(Me)₂ n-Heptyl (R)- V-369 Me Me Me NH Ph CH₂C(Me)₂ n-Undecyl racemic V-370 Me Me Me NH Ph CH₂C(Me)₂ n-Undecyl (R)- V-371 Me Et Me NH Ph CH₂C(Me)₂ n-Undecyl racemic V-372 Me Et Me NH Ph CH₂C(Me)₂ n-Undecyl (R)- V-373 Me Me Me NH Ph CH₂C(Me)₂ Ph racemic V-374 Me Me Me NH Ph CH₂C(Me)₂ Ph (R)- V-375 Me Et Me NH Ph CH₂C(Me)₂ Ph racemic V-376 Me Et Me NH Ph CH₂C(Me)₂ Ph (R)- V-377 Me Me Me NH Ph CH₂C(Me)₂ OEt racemic V-378 Me Me Me NH Ph CH₂C(Me)₂ OEt (R)- V-379 Me Et Me NH Ph CH₂C(Me)₂ OEt racemic V-380 Me Et Me NH Ph CH₂C(Me)₂ OEt (R)- V-381 Me Me Me NH Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-382 Me Me Me NH Ph CH₂C(Me)₂ (CH₂)₂COOH (R)- V-383 Me Et Me NH Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-384 Me Et Me NH Ph CH₂C(Me)₂ (CH₂)₂COOH (R)- V-385 Me Me Me CH₂ Ph CH₂ Me racemic V-386 Me Me Me CH₂ Ph CH₂ Me (S)- V-387 Me Et Me CH₂ Ph CH₂ Me racemic V-388 Me Et Me CH₂ Ph CH₂ Me (S)- V-389 Me Me Me CH₂ Ph CH₂ Et racemic V-390 Me Me Me CH₂ Ph CH₂ Et (S)- V-391 Me Et Me CH₂ Ph CH₂ Et racemic V-392 Me Et Me CH₂ Ph CH₂ Et (S)- V-393 Me Me Me CH₂ Ph CH₂ nPr racemic V-394 Me Me Me CH₂ Ph CH₂ nPr (S)- V-395 Me Et Me CH₂ Ph CH₂ nPr racemic V-396 Me Et Me CH₂ Ph CH₂ nPr (S)- V-397 Me Me Me CH₂ Ph CH₂ iPr racemic V-398 Me Me Me CH₂ Ph CH₂ iPr (S)- V-399 Me Et Me CH₂ Ph CH₂ iPr racemic V-400 Me Et Me CH₂ Ph CH₂ iPr (S)-

TABLE 107 (Va)

Com- pound No. R¹ R² R³ L² R⁴ L³ R⁶ Configuration V-401 Me Me Me CH₂ Ph CH₂ nBu racemic V-402 Me Me Me CH₂ Ph CH₂ nBu (S)- V-403 Me Et Me CH₂ Ph CH₂ nBu racemic V-404 Me Et Me CH₂ Ph CH₂ nBu (S)- V-405 Me Me Me CH₂ Ph CH₂ tBu racemic V-406 Me Me Me CH₂ Ph CH₂ tBu (S)- V-407 Me Et Me CH₂ Ph CH₂ tBu racemic V-408 Me Et Me CH₂ Ph CH₂ tBu (S)- V-409 Me Me Me CH₂ Ph CH₂ iBu racemic V-410 Me Me Me CH₂ Ph CH₂ iBu (S)- V-411 Me Et Me CH₂ Ph CH₂ iBu racemic V-412 Me Et Me CH₂ Ph CH₂ iBu (S)- V-413 Me Me Me CH₂ Ph CH₂ n-Heptyl racemic V-414 Me Me Me CH₂ Ph CH₂ n-Heptyl (S)- V-415 Me Et Me CH₂ Ph CH₂ n-Heptyl racemic V-416 Me Et Me CH₂ Ph CH₂ n-Heptyl (S)- V-417 Me Me Me CH₂ Ph CH₂ n-Undecyl racemic V-418 Me Me Me CH₂ Ph CH₂ n-Undecyl (S)- V-419 Me Et Me CH₂ Ph CH₂ n-Undecyl racemic V-420 Me Et Me CH₂ Ph CH₂ n-Undecyl (S)- V-421 Me Me Me CH₂ Ph CH₂ Ph racemic V-422 Me Me Me CH₂ Ph CH₂ Ph (S)- V-423 Me Et Me CH₂ Ph CH₂ Ph racemic V-424 Me Et Me CH₂ Ph CH₂ Ph (S)- V-425 Me Me Me CH₂ Ph CH₂ OEt racemic V-426 Me Me Me CH₂ Ph CH₂ OEt (S)- V-427 Me Et Me CH₂ Ph CH₂ OEt racemic V-428 Me Et Me CH₂ Ph CH₂ OEt (S)- V-429 Me Me Me CH₂ Ph CH₂ (CH₂)₂COOH racemic V-430 Me Me Me CH₂ Ph CH₂ (CH₂)₂COOH (S)- V-431 Me Et Me CH₂ Ph CH₂ (CH₂)₂COOH racemic V-432 Me Et Me CH₂ Ph CH₂ (CH₂)₂COOH (S)- V-433 Me Me Me CH₂ Ph — Me racemic V-434 Me Me Me CH₂ Ph — Me (S)- V-435 Me Et Me CH₂ Ph — Me racemic V-436 Me Et Me CH₂ Ph — Me (S)- V-437 Me Me Me CH₂ Ph — Et racemic V-438 Me Me Me CH₂ Ph — Et (S)- V-439 Me Et Me CH₂ Ph — Et racemic V-440 Me Et Me CH₂ Ph — Et (S)- V-441 Me Me Me CH₂ Ph — nPr racemic V-442 Me Me Me CH₂ Ph — nPr (S)- V-443 Me Et Me CH₂ Ph — nPr racemic V-444 Me Et Me CH₂ Ph — nPr (S)- V-445 Me Me Me CH₂ Ph — iPr racemic V-446 Me Me Me CH₂ Ph — iPr (S)- V-447 Me Et Me CH₂ Ph — iPr racemic V-448 Me Et Me CH₂ Ph — iPr (S)- V-449 Me Me Me CH₂ Ph — nBu racemic V-450 Me Me Me CH₂ Ph — nBu (S)-

TABLE 108 (Va)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-451 Me Et Me CH₂ Ph — nBu racemic V-452 Me Et Me CH₂ Ph — nBu (S)- V-453 Me Me Me CH₂ Ph — tBu racemic V-454 Me Me Me CH₂ Ph — tBu (S)- V-455 Me Et Me CH₂ Ph — tBu racemic V-456 Me Et Me CH₂ Ph — tBu (S)- V-457 Me Me Me CH₂ Ph — iBu racemic V-458 Me Me Me CH₂ Ph — iBu (S)- V-459 Me Et Me CH₂ Ph — iBu racemic V-460 Me Et Me CH₂ Ph — iBu (S)- V-461 Me Me Me CH₂ Ph — n-Heptyl racemic V-462 Me Me Me CH₂ Ph — n-Heptyl (S)- V-463 Me Et Me CH₂ Ph — n-Heptyl racemic V-464 Me Et Me CH₂ Ph — n-Heptyl (S)- V-465 Me Me Me CH₂ Ph — n-Undecyl racemic V-466 Me Me Me CH₂ Ph — n-Undecyl (S)- V-467 Me Et Me CH₂ Ph — n-Undecyl racemic V-468 Me Et Me CH₂ Ph — n-Undecyl (S)- V-469 Me Me Me CH₂ Ph — Ph racemic V-470 Me Me Me CH₂ Ph — Ph (S)- V-471 Me Et Me CH₂ Ph — Ph racemic V-472 Me Et Me CH₂ Ph — Ph (S)- V-473 Me Me Me CH₂ Ph — OEt racemic V-474 Me Me Me CH₂ Ph — OEt (S)- V-475 Me Et Me CH₂ Ph — OEt racemic V-476 Me Et Me CH₂ Ph — OEt (S)- V-477 Me Me Me CH₂ Ph — (CH₂)₂COOH racemic V-478 Me Me Me CH₂ Ph — (CH₂)₂COOH (S)- V-479 Me Et Me CH₂ Ph — (CH₂)₂COOH racemic V-480 Me Et Me CH₂ Ph — (CH₂)₂COOH (S)- V-481 Me Me Me CH₂ Ph C(Me)₂ Me racemic V-482 Me Me Me CH₂ Ph C(Me)₂ Me (S)- V-483 Me Et Me CH₂ Ph C(Me)₂ Me racemic V-484 Me Et Me CH₂ Ph C(Me)₂ Me (S)- V-485 Me Me Me CH₂ Ph C(Me)₂ Et racemic V-486 Me Me Me CH₂ Ph C(Me)₂ Et (S)- V-487 Me Et Me CH₂ Ph C(Me)₂ Et racemic V-488 Me Et Me CH₂ Ph C(Me)₂ Et (S)- V-489 Me Me Me CH₂ Ph C(Me)₂ nPr racemic V-490 Me Me Me CH₂ Ph C(Me)₂ nPr (S)- V-491 Me Et Me CH₂ Ph C(Me)₂ nPr racemic V-492 Me Et Me CH₂ Ph C(Me)₂ nPr (S)- V-493 Me Me Me CH₂ Ph C(Me)₂ iPr racemic V-494 Me Me Me CH₂ Ph C(Me)₂ iPr (S)- V-495 Me Et Me CH₂ Ph C(Me)₂ iPr racemic V-496 Me Et Me CH₂ Ph C(Me)₂ iPr (S)- V-497 Me Me Me CH₂ Ph C(Me)₂ nBu racemic V-498 Me Me Me CH₂ Ph C(Me)₂ nBu (S)- V-499 Me Et Me CH₂ Ph C(Me)₂ nBu racemic V-500 Me Et Me CH₂ Ph C(Me)₂ nBu (S)-

TABLE 109 (Va)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-501 Me Me Me CH₂ Ph C(Me)₂ tBu racemic V-502 Me Me Me CH₂ Ph C(Me)₂ tBu (S)- V-503 Me Et Me CH₂ Ph C(Me)₂ tBu racemic V-504 Me Et Me CH₂ Ph C(Me)₂ tBu (S)- V-505 Me Me Me CH₂ Ph C(Me)₂ iBu racemic V-506 Me Me Me CH₂ Ph C(Me)₂ iBu (S)- V-507 Me Et Me CH₂ Ph C(Me)₂ iBu racemic V-508 Me Et Me CH₂ Ph C(Me)₂ iBu (S)- V-509 Me Me Me CH₂ Ph C(Me)₂ n-Heptyl racemic V-510 Me Me Me CH₂ Ph C(Me)₂ n-Heptyl (S)- V-511 Me Et Me CH₂ Ph C(Me)₂ n-Heptyl racemic V-512 Me Et Me CH₂ Ph C(Me)₂ n-Heptyl (S)- V-513 Me Me Me CH₂ Ph C(Me)₂ n-Undecyl racemic V-514 Me Me Me CH₂ Ph C(Me)₂ n-Undecyl (S)- V-515 Me Et Me CH₂ Ph C(Me)₂ n-Undecyl racemic V-516 Me Et Me CH₂ Ph C(Me)₂ n-Undecyl (S)- V-517 Me Me Me CH₂ Ph C(Me)₂ Ph racemic V-518 Me Me Me CH₂ Ph C(Me)₂ Ph (S)- V-519 Me Et Me CH₂ Ph C(Me)₂ Ph racemic V-520 Me Et Me CH₂ Ph C(Me)₂ Ph (S)- V-521 Me Me Me CH₂ Ph C(Me)₂ OEt racemic V-522 Me Me Me CH₂ Ph C(Me)₂ OEt (S)- V-523 Me Et Me CH₂ Ph C(Me)₂ OEt racemic V-524 Me Et Me CH₂ Ph C(Me)₂ OEt (S)- V-525 Me Me Me CH₂ Ph C(Me)₂ (CH₂)₂COOH racemic V-526 Me Me Me CH₂ Ph C(Me)₂ (CH₂)₂COOH (S)- V-527 Me Et Me CH₂ Ph C(Me)₂ (CH₂)₂COOH racemic V-528 Me Et Me CH₂ Ph C(Me)₂ (CH₂)₂COOH (S)- V-529 Me Me Me CH₂ Ph (CH₂)₂ Me racemic V-530 Me Me Me CH₂ Ph (CH₂)₂ Me (S)- V-531 Me Et Me CH₂ Ph (CH₂)₂ Me racemic V-532 Me Et Me CH₂ Ph (CH₂)₂ Me (S)- V-533 Me Me Me CH₂ Ph (CH₂)₂ Et racemic V-534 Me Me Me CH₂ Ph (CH₂)₂ Et (S)- V-535 Me Et Me CH₂ Ph (CH₂)₂ Et racemic V-536 Me Et Me CH₂ Ph (CH₂)₂ Et (S)- V-537 Me Me Me CH₂ Ph (CH₂)₂ nPr racemic V-538 Me Me Me CH₂ Ph (CH₂)₂ nPr (S)- V-539 Me Et Me CH₂ Ph (CH₂)₂ nPr racemic V-540 Me Et Me CH₂ Ph (CH₂)₂ nPr (S)- V-541 Me Me Me CH₂ Ph (CH₂)₂ iPr racemic V-542 Me Me Me CH₂ Ph (CH₂)₂ iPr (S)- V-543 Me Et Me CH₂ Ph (CH₂)₂ iPr racemic V-544 Me Et Me CH₂ Ph (CH₂)₂ iPr (S)- V-545 Me Me Me CH₂ Ph (CH₂)₂ nBu racemic V-546 Me Me Me CH₂ Ph (CH₂)₂ nBu (S)- V-547 Me Et Me CH₂ Ph (CH₂)₂ nBu racemic V-548 Me Et Me CH₂ Ph (CH₂)₂ nBu (S)- V-549 Me Me Me CH₂ Ph (CH₂)₂ tBu racemic V-550 Me Me Me CH₂ Ph (CH₂)₂ tBu (S)-

TABLE 110 (Va)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-551 Me Et Me CH₂ Ph (CH₂)₂ tBu racemic V-552 Me Et Me CH₂ Ph (CH₂)₂ tBu (S)- V-553 Me Me Me CH₂ Ph (CH₂)₂ iBu racemic V-554 Me Me Me CH₂ Ph (CH₂)₂ iBu (S)- V-555 Me Et Me CH₂ Ph (CH₂)₂ iBu racemic V-556 Me Et Me CH₂ Ph (CH₂)₂ iBu (S)- V-557 Me Me Me CH₂ Ph (CH₂)₂ n-Heptyl racemic V-558 Me Me Me CH₂ Ph (CH₂)₂ n-Heptyl (S)- V-559 Me Et Me CH₂ Ph (CH₂)₂ n-Heptyl racemic V-560 Me Et Me CH₂ Ph (CH₂)₂ n-Heptyl (S)- V-561 Me Me Me CH₂ Ph (CH₂)₂ n-Undecyl racemic V-562 Me Me Me CH₂ Ph (CH₂)₂ n-Undecyl (S)- V-563 Me Et Me CH₂ Ph (CH₂)₂ n-Undecyl racemic V-564 Me Et Me CH₂ Ph (CH₂)₂ n-Undecyl (S)- V-565 Me Me Me CH₂ Ph (CH₂)₂ Ph racemic V-566 Me Me Me CH₂ Ph (CH₂)₂ Ph (S)- V-567 Me Et Me CH₂ Ph (CH₂)₂ Ph racemic V-568 Me Et Me CH₂ Ph (CH₂)₂ Ph (S)- V-569 Me Me Me CH₂ Ph (CH₂)₂ OEt racemic V-570 Me Me Me CH₂ Ph (CH₂)₂ OEt (S)- V-571 Me Et Me CH₂ Ph (CH₂)₂ OEt racemic V-572 Me Et Me CH₂ Ph (CH₂)₂ OEt (S)- V-573 Me Me Me CH₂ Ph (CH₂)₂ (CH₂)₂COOH racemic V-574 Me Me Me CH₂ Ph (CH₂)₂ (CH₂)₂COOH (S)- V-575 Me Et Me CH₂ Ph (CH₂)₂ (CH₂)₂COOH racemic V-576 Me Et Me CH₂ Ph (CH₂)₂ (CH₂)₂COOH (S)- V-577 Me Me Me CH₂ Ph CH₂C(Me)₂ Me racemic V-578 Me Me Me CH₂ Ph CH₂C(Me)₂ Me (S)- V-579 Me Et Me CH₂ Ph CH₂C(Me)₂ Me racemic V-580 Me Et Me CH₂ Ph CH₂C(Me)₂ Me (S)- V-581 Me Me Me CH₂ Ph CH₂C(Me)₂ Et racemic V-582 Me Me Me CH₂ Ph CH₂C(Me)₂ Et (S)- V-583 Me Et Me CH₂ Ph CH₂C(Me)₂ Et racemic V-584 Me Et Me CH₂ Ph CH₂C(Me)₂ Et (S)- V-585 Me Me Me CH₂ Ph CH₂C(Me)₂ nPr racemic V-586 Me Me Me CH₂ Ph CH₂C(Me)₂ nPr (S)- V-587 Me Et Me CH₂ Ph CH₂C(Me)₂ nPr racemic V-588 Me Et Me CH₂ Ph CH₂C(Me)₂ nPr (S)- V-589 Me Me Me CH₂ Ph CH₂C(Me)₂ iPr racemic V-590 Me Me Me CH₂ Ph CH₂C(Me)₂ iPr (S)- V-591 Me Et Me CH₂ Ph CH₂C(Me)₂ iPr racemic V-592 Me Et Me CH₂ Ph CH₂C(Me)₂ iPr (S)- V-593 Me Me Me CH₂ Ph CH₂C(Me)₂ nBu racemic V-594 Me Me Me CH₂ Ph CH₂C(Me)₂ nBu (S)- V-595 Me Et Me CH₂ Ph CH₂C(Me)₂ nBu racemic V-596 Me Et Me CH₂ Ph CH₂C(Me)₂ nBu (S)- V-597 Me Me Me CH₂ Ph CH₂C(Me)₂ tBu racemic V-598 Me Me Me CH₂ Ph CH₂C(Me)₂ tBu (S)- V-599 Me Et Me CH₂ Ph CH₂C(Me)₂ tBu racemic V-600 Me Et Me CH₂ Ph CH₂C(Me)₂ tBu (S)-

TABLE 111 (Va)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-601 Me Me Me CH₂ Ph CH₂C(Me)₂ iBu racemic V-602 Me Me Me CH₂ Ph CH₂C(Me)₂ iBu (S)- V-603 Me Et Me CH₂ Ph CH₂C(Me)₂ iBu racemic V-604 Me Et Me CH₂ Ph CH₂C(Me)₂ iBu (S)- V-605 Me Me Me CH₂ Ph CH₂C(Me)₂ n-Heptyl racemic V-606 Me Me Me CH₂ Ph CH₂C(Me)₂ n-Heptyl (S)- V-607 Me Et Me CH₂ Ph CH₂C(Me)₂ n-Heptyl racemic V-608 Me Et Me CH₂ Ph CH₂C(Me)₂ n-Heptyl (S)- V-609 Me Me Me CH₂ Ph CH₂C(Me)₂ n-Undecyl racemic V-610 Me Me Me CH₂ Ph CH₂C(Me)₂ n-Undecyl (S)- V-611 Me Et Me CH₂ Ph CH₂C(Me)₂ n-Undecyl racemic V-612 Me Et Me CH₂ Ph CH₂C(Me)₂ n-Undecyl (S)- V-613 Me Me Me CH₂ Ph CH₂C(Me)₂ Ph racemic V-614 Me Me Me CH₂ Ph CH₂C(Me)₂ Ph (S)- V-615 Me Et Me CH₂ Ph CH₂C(Me)₂ Ph racemic V-616 Me Et Me CH₂ Ph CH₂C(Me)₂ Ph (S)- V-617 Me Me Me CH₂ Ph CH₂C(Me)₂ OEt racemic V-618 Me Me Me CH₂ Ph CH₂C(Me)₂ OEt (S)- V-619 Me Et Me CH₂ Ph CH₂C(Me)₂ OEt racemic V-620 Me Et Me CH₂ Ph CH₂C(Me)₂ OEt (S)- V-621 Me Me Me CH₂ Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-622 Me Me Me CH₂ Ph CH₂C(Me)₂ (CH₂)₂COOH (S)- V-623 Me Et Me CH₂ Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-624 Me Et Me CH₂ Ph CH₂C(Me)₂ (CH₂)₂COOH (S)-

TABLE 112 (Va)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-1884 Me Me Me — Ph — Me racemic V-1885 Me Me Me — Ph — Me (R)- V-1886 Me Et Me — Ph — Me racemic V-1887 Me Et Me — Ph — Me (R)- V-1888 Me Me Me — Ph — Et racemic V-1889 Me Me Me — Ph — Et (R)- V-1890 Me Et Me — Ph — Et racemic V-1891 Me Et Me — Ph — Et (R)- V-1892 Me Me Me — Ph — nPr racemic V-1893 Me Me Me — Ph — nPr (R)- V-1894 Me Et Me — Ph — nPr racemic V-1895 Me Et Me — Ph — nPr (R)- V-1896 Me Me Me — Ph — iPr racemic V-1897 Me Me Me — Ph — iPr (R)- V-1898 Me Et Me — Ph — iPr racemic V-1899 Me Et Me — Ph — iPr (R)- V-1900 Me Me Me — Ph — nBu racemic V-1901 Me Me Me — Ph — nBu (R)- V-1902 Me Et Me — Ph — nBu racemic V-1903 Me Et Me — Ph — nBu (R)- V-1904 Me Me Me — Ph — tBu racemic V-1905 Me Me Me — Ph — tBu (R)- V-1906 Me Et Me — Ph — tBu racemic V-1907 Me Et Me — Ph — tBu (R)- V-1908 Me Me Me — Ph — iBu racemic V-1909 Me Me Me — Ph — iBu (R)- V-1910 Me Et Me — Ph — iBu racemic V-1911 Me Et Me — Ph — iBu (R)- V-1912 Me Me Me — Ph — n-Heptyl racemic V-1913 Me Me Me — Ph — n-Heptyl (R)- V-1914 Me Et Me — Ph — n-Heptyl racemic V-1915 Me Et Me — Ph — n-Heptyl (R)- V-1916 Me Me Me — Ph — n-Undecyl racemic V-1917 Me Me Me — Ph — n-Undecyl (R)- V-1918 Me Et Me — Ph — n-Undecyl racemic V-1919 Me Et Me — Ph — n-Undecyl (R)- V-1920 Me Me Me — Ph — OEt racemic V-1921 Me Me Me — Ph — OEt (R)- V-1922 Me Et Me — Ph — OEt racemic V-1923 Me Et Me — Ph — OEt (R)- V-1924 Me Me Me — Ph — (CH₂)₂COONa racemic V-1925 Me Me Me — Ph — (CH₂)₂COONa (R)- V-1926 Me Et Me — Ph — (CH₂)₂COONa racemic V-1927 Me Et Me — Ph — (CH₂)₂COONa (R)- V-1928 Me Me Me — Ph CH₂ Me racemic V-1929 Me Me Me — Ph CH₂ Me (S)- V-1930 Me Et Me — Ph CH₂ Me racemic V-1931 Me Et Me — Ph CH₂ Me (S)- V-1932 Me Me Me — Ph CH₂ Et racemic V-1933 Me Me Me — Ph CH₂ Et (S)-

TABLE 113 (Va)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-1934 Me Et Me — Ph CH₂ Et racemic V-1935 Me Et Me — Ph CH₂ Et (S)- V-1936 Me Me Me — Ph CH₂ nPr racemic V-1937 Me Me Me — Ph CH₂ nPr (S)- V-1938 Me Et Me — Ph CH₂ nPr racemic V-1939 Me Et Me — Ph CH₂ nPr (S)- V-1940 Me Me Me — Ph CH₂ iPr racemic V-1941 Me Me Me — Ph CH₂ iPr (S)- V-1942 Me Et Me — Ph CH₂ iPr racemic V-1943 Me Et Me — Ph CH₂ iPr (S)- V-1944 Me Me Me — Ph CH₂ nBu racemic V-1945 Me Me Me — Ph CH₂ nBu (S)- V-1946 Me Et Me — Ph CH₂ nBu racemic V-1947 Me Et Me — Ph CH₂ nBu (S)- V-1948 Me Me Me — Ph CH₂ tBu racemic V-1949 Me Me Me — Ph CH₂ tBu (S)- V-1950 Me Et Me — Ph CH₂ tBu racemic V-1951 Me Et Me — Ph CH₂ tBu (S)- V-1952 Me Me Me — Ph CH₂ iBu racemic V-1953 Me Me Me — Ph CH₂ iBu (S)- V-1954 Me Et Me — Ph CH₂ iBu racemic V-1955 Me Et Me — Ph CH₂ iBu (S)- V-1956 Me Me Me — Ph CH₂ n-Heptyl racemic V-1957 Me Me Me — Ph CH₂ n-Heptyl (S)- V-1958 Me Et Me — Ph CH₂ n-Heptyl racemic V-1959 Me Et Me — Ph CH₂ n-Heptyl (S)- V-1960 Me Me Me — Ph CH₂ n-Undecyl racemic V-1961 Me Me Me — Ph CH₂ n-Undecyl (S)- V-1962 Me Et Me — Ph CH₂ n-Undecyl racemic V-1963 Me Et Me — Ph CH₂ n-Undecyl (S)- V-1964 Me Me Me — Ph CH₂ OEt racemic V-1965 Me Me Me — Ph CH₂ OEt (S)- V-1966 Me Et Me — Ph CH₂ OEt racemic V-1967 Me Et Me — Ph CH₂ OEt (S)- V-1968 Me Me Me — Ph CH₂ (CH₂)₂COONa racemic V-1969 Me Me Me — Ph CH₂ (CH₂)₂COONa (S)- V-1970 Me Et Me — Ph CH₂ (CH₂)₂COONa racemic V-1971 Me Et Me — Ph CH₂ (CH₂)₂COONa (S)-

TABLE 114 (Vb)

Com- pound Configura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-625 Me Me Me O Ph CH₂ Me racemic V-626 Me Me Me O Ph CH₂ Me (S)- V-627 Me Et Me O Ph CH₂ Me racemic V-628 Me Et Me O Ph CH₂ Me (S)- V-629 Me Me Me O Ph CH₂ Et racemic V-630 Me Me Me O Ph CH₂ Et (S)- V-631 Me Et Me O Ph CH₂ Et racemic V-632 Me Et Me O Ph CH₂ Et (S)- V-633 Me Me Me O Ph CH₂ nPr racemic V-634 Me Me Me O Ph CH₂ nPr (S)- V-635 Me Et Me O Ph CH₂ nPr racemic V-636 Me Et Me O Ph CH₂ nPr (S)- V-637 Me Me Me O Ph CH₂ iPr racemic V-638 Me Me Me O Ph CH₂ iPr (S)- V-639 Me Et Me O Ph CH₂ iPr racemic V-640 Me Et Me O Ph CH₂ iPr (S)- V-641 Me Me Me O Ph CH₂ nBu racemic V-642 Me Me Me O Ph CH₂ nBu (S)- V-643 Me Et Me O Ph CH₂ nBu racemic V-644 Me Et Me O Ph CH₂ nBu (S)- V-645 Me Me Me O Ph CH₂ tBu racemic V-646 Me Me Me O Ph CH₂ tBu (S)- V-647 Me Et Me O Ph CH₂ tBu racemic V-648 Me Et Me O Ph CH₂ tBu (S)- V-649 Me Me Me O Ph CH₂ iBu racemic V-650 Me Me Me O Ph CH₂ iBu (S)- V-651 Me Et Me O Ph CH₂ iBu racemic V-652 Me Et Me O Ph CH₂ iBu (S)- V-653 Me Me Me O Ph CH₂ n-Heptyl racemic V-654 Me Me Me O Ph CH₂ n-Heptyl (S)- V-655 Me Et Me O Ph CH₂ n-Heptyl racemic V-656 Me Et Me O Ph CH₂ n-Heptyl (S)- V-657 Me Me Me O Ph CH₂ n-Undecyl racemic V-658 Me Me Me O Ph CH₂ n-Undecyl (S)- V-659 Me Et Me O Ph CH₂ n-Undecyl racemic V-660 Me Et Me O Ph CH₂ n-Undecyl (S)- V-661 Me Me Me O Ph CH₂ Ph racemic V-662 Me Me Me O Ph CH₂ Ph (S)- V-663 Me Et Me O Ph CH₂ Ph racemic V-664 Me Et Me O Ph CH₂ Ph (S)- V-665 Me Me Me O Ph CH₂ OEt racemic V-666 Me Me Me O Ph CH₂ OEt (S)- V-667 Me Et Me O Ph CH₂ OEt racemic V-668 Me Et Me O Ph CH₂ OEt (S)- V-669 Me Me Me O Ph CH₂ (CH₂)₂COOH racemic V-670 Me Me Me O Ph CH₂ (CH₂)₂COOH (S)- V-671 Me Et Me O Ph CH₂ (CH₂)₂COOH racemic V-672 Me Et Me O Ph CH₂ (CH₂)₂COOH (S)- V-673 Me Me Me O Ph C(Me)₂ Me racemic V-674 Me Me Me O Ph C(Me)₂ Me (S)- V-675 Me Et Me O Ph C(Me)₂ Me racemic

TABLE 115 (Vb)

Com- pound Configura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-676 Me Et Me O Ph C(Me)₂ Me (S)- V-677 Me Me Me O Ph C(Me)₂ Et racemic V-678 Me Me Me O Ph C(Me)₂ Et (S)- V-679 Me Et Me O Ph C(Me)₂ Et racemic V-680 Me Et Me O Ph C(Me)₂ Et (S)- V-681 Me Me Me O Ph C(Me)₂ nPr racemic V-682 Me Me Me O Ph C(Me)₂ nPr (S)- V-683 Me Et Me O Ph C(Me)₂ nPr racemic V-684 Me Et Me O Ph C(Me)₂ nPr (S)- V-685 Me Me Me O Ph C(Me)₂ iPr racemic V-686 Me Me Me O Ph C(Me)₂ iPr (S)- V-687 Me Et Me O Ph C(Me)₂ iPr racemic V-688 Me Et Me O Ph C(Me)₂ iPr (S)- V-689 Me Me Me O Ph C(Me)₂ nBu racemic V-690 Me Me Me O Ph C(Me)₂ nBu (S)- V-691 Me Et Me O Ph C(Me)₂ nBu racemic V-692 Me Et Me O Ph C(Me)₂ nBu (S)- V-693 Me Me Me O Ph C(Me)₂ tBu racemic V-694 Me Me Me O Ph C(Me)₂ tBu (S)- V-695 Me Et Me O Ph C(Me)₂ tBu racemic V-696 Me Et Me O Ph C(Me)₂ tBu (S)- V-697 Me Me Me O Ph C(Me)₂ iBu racemic V-698 Me Me Me O Ph C(Me)₂ iBu (S)- V-699 Me Et Me O Ph C(Me)₂ iBu racemic V-700 Me Et Me O Ph C(Me)₂ iBu (S)- V-701 Me Me Me O Ph C(Me)₂ n-Heptyl racemic V-702 Me Me Me O Ph C(Me)₂ n-Heptyl (S)- V-703 Me Et Me O Ph C(Me)₂ n-Heptyl racemic V-704 Me Et Me O Ph C(Me)₂ n-Heptyl (S)- V-705 Me Me Me O Ph C(Me)₂ n-Undecyl racemic V-706 Me Me Me O Ph C(Me)₂ n-Undecyl (S)- V-707 Me Et Me O Ph C(Me)₂ n-Undecyl racemic V-708 Me Et Me O Ph C(Me)₂ n-Undecyl (S)- V-709 Me Me Me O Ph C(Me)₂ Ph racemic V-710 Me Me Me O Ph C(Me)₂ Ph (S)- V-711 Me Et Me O Ph C(Me)₂ Ph racemic V-712 Me Et Me O Ph C(Me)₂ Ph (S)- V-713 Me Me Me O Ph C(Me)₂ OEt racemic V-714 Me Me Me O Ph C(Me)₂ OEt (S)- V-715 Me Et Me O Ph C(Me)₂ OEt racemic V-716 Me Et Me O Ph C(Me)₂ OEt (S)- V-717 Me Me Me O Ph C(Me)₂ (CH₂)₂COOH racemic V-718 Me Me Me O Ph C(Me)₂ (CH₂)₂COOH (S)- V-719 Me Et Me O Ph C(Me)₂ (CH₂)₂COOH racemic V-720 Me Et Me O Ph C(Me)₂ (CH₂)₂COOH (S)- V-721 Me Me Me O Ph (CH₂)₂ Me racemic V-722 Me Me Me O Ph (CH₂)₂ Me (R)- V-723 Me Et Me O Ph (CH₂)₂ Me racemic V-724 Me Et Me O Ph (CH₂)₂ Me (R)- V-725 Me Me Me O Ph (CH₂)₂ Et racemic

TABLE 116 (Vb)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-726 Me Me Me O Ph (CH₂)₂ Et (R)- V-727 Me Et Me O Ph (CH₂)₂ Et racemic V-728 Me Et Me O Ph (CH₂)₂ Et (R)- V-729 Me Me Me O Ph (CH₂)₂ nPr racemic V-730 Me Me Me O Ph (CH₂)₂ nPr (R)- V-731 Me Et Me O Ph (CH₂)₂ nPr racemic V-732 Me Et Me O Ph (CH₂)₂ nPr (R)- V-733 Me Me Me O Ph (CH₂)₂ iPr racemic V-734 Me Me Me O Ph (CH₂)₂ iPr (R)- V-735 Me Et Me O Ph (CH₂)₂ iPr racemic V-736 Me Et Me O Ph (CH₂)₂ iPr (R)- V-737 Me Me Me O Ph (CH₂)₂ nBu racemic V-738 Me Me Me O Ph (CH₂)₂ nBu (R)- V-739 Me Et Me O Ph (CH₂)₂ nBu racemic V-740 Me Et Me O Ph (CH₂)₂ nBu (R)- V-741 Me Me Me O Ph (CH₂)₂ tBu racemic V-742 Me Me Me O Ph (CH₂)₂ tBu (R)- V-743 Me Et Me O Ph (CH₂)₂ tBu racemic V-744 Me Et Me O Ph (CH₂)₂ tBu (R)- V-745 Me Me Me O Ph (CH₂)₂ iBu racemic V-746 Me Me Me O Ph (CH₂)₂ iBu (R)- V-747 Me Et Me O Ph (CH₂)₂ iBu racemic V-748 Me Et Me O Ph (CH₂)₂ iBu (R)- V-749 Me Me Me O Ph (CH₂)₂ n-Heptyl racemic V-750 Me Me Me O Ph (CH₂)₂ n-Heptyl (R)- V-751 Me Et Me O Ph (CH₂)₂ n-Heptyl racemic V-752 Me Et Me O Ph (CH₂)₂ n-Heptyl (R)- V-753 Me Me Me O Ph (CH₂)₂ n-Undecyl racemic V-754 Me Me Me O Ph (CH₂)₂ n-Undecyl (R)- V-755 Me Et Me O Ph (CH₂)₂ n-Undecyl racemic V-756 Me Et Me O Ph (CH₂)₂ n-Undecyl (R)- V-757 Me Me Me O Ph (CH₂)₂ Ph racemic V-758 Me Me Me O Ph (CH₂)₂ Ph (R)- V-759 Me Et Me O Ph (CH₂)₂ Ph racemic V-760 Me Et Me O Ph (CH₂)₂ Ph (R)- V-761 Me Me Me O Ph (CH₂)₂ OEt racemic V-762 Me Me Me O Ph (CH₂)₂ OEt (R)- V-763 Me Et Me O Ph (CH₂)₂ OEt racemic V-764 Me Et Me O Ph (CH₂)₂ OEt (R)- V-765 Me Me Me O Ph (CH₂)₂ (CH₂)₂COOH racemic V-766 Me Me Me O Ph (CH₂)₂ (CH₂)₂COOH (R)- V-767 Me Et Me O Ph (CH₂)₂ (CH₂)₂COOH racemic V-768 Me Et Me O Ph (CH₂)₂ (CH₂)₂COOH (R)- V-769 Me Me Me O Ph CH₂C(Me)₂ Me racemic V-770 Me Me Me O Ph CH₂C(Me)₂ Me (R)- V-771 Me Et Me O Ph CH₂C(Me)₂ Me racemic V-772 Me Et Me O Ph CH₂C(Me)₂ Me (R)- V-773 Me Me Me O Ph CH₂C(Me)₂ Et racemic V-774 Me Me Me O Ph CH₂C(Me)₂ Et (R)- V-775 Me Et Me O Ph CH₂C(Me)₂ Et racemic

TABLE 117 (Vb)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-776 Me Et Me O Ph CH₂C(Me)₂ Et (R)- V-777 Me Me Me O Ph CH₂C(Me)₂ nPr racemic V-778 Me Me Me O Ph CH₂C(Me)₂ nPr (R)- V-779 Me Et Me O Ph CH₂C(Me)₂ nPr racemic V-780 Me Et Me O Ph CH₂C(Me)₂ nPr (R)- V-781 Me Me Me O Ph CH₂C(Me)₂ iPr racemic V-782 Me Me Me O Ph CH₂C(Me)₂ iPr (R)- V-783 Me Et Me O Ph CH₂C(Me)₂ iPr racemic V-784 Me Et Me O Ph CH₂C(Me)₂ iPr (R)- V-785 Me Me Me O Ph CH₂C(Me)₂ nBu racemic V-786 Me Me Me O Ph CH₂C(Me)₂ nBu (R)- V-787 Me Et Me O Ph CH₂C(Me)₂ nBu racemic V-788 Me Et Me O Ph CH₂C(Me)₂ nBu (R)- V-789 Me Me Me O Ph CH₂C(Me)₂ tBu racemic V-790 Me Me Me O Ph CH₂C(Me)₂ tBu (R)- V-791 Me Et Me O Ph CH₂C(Me)₂ tBu racemic V-792 Me Et Me O Ph CH₂C(Me)₂ tBu (R)- V-793 Me Me Me O Ph CH₂C(Me)₂ iBu racemic V-794 Me Me Me O Ph CH₂C(Me)₂ iBu (R)- V-795 Me Et Me O Ph CH₂C(Me)₂ iBu racemic V-796 Me Et Me O Ph CH₂C(Me)₂ iBu (R)- V-797 Me Me Me O Ph CH₂C(Me)₂ n-Heptyl racemic V-798 Me Me Me O Ph CH₂C(Me)₂ n-Heptyl (R)- V-799 Me Et Me O Ph CH₂C(Me)₂ n-Heptyl racemic V-800 Me Et Me O Ph CH₂C(Me)₂ n-Heptyl (R)- V-801 Me Me Me O Ph CH₂C(Me)₂ n-Undecyl racemic V-802 Me Me Me O Ph CH₂C(Me)₂ n-Undecyl (R)- V-803 Me Et Me O Ph CH₂C(Me)₂ n-Undecyl racemic V-804 Me Et Me O Ph CH₂C(Me)₂ n-Undecyl (R)- V-805 Me Me Me O Ph CH₂C(Me)₂ Ph racemic V-806 Me Me Me O Ph CH₂C(Me)₂ Ph (R)- V-807 Me Et Me O Ph CH₂C(Me)₂ Ph racemic V-808 Me Et Me O Ph CH₂C(Me)₂ Ph (R)- V-809 Me Me Me O Ph CH₂C(Me)₂ OEt racemic V-810 Me Me Me O Ph CH₂C(Me)₂ OEt (R)- V-811 Me Et Me O Ph CH₂C(Me)₂ OEt racemic V-812 Me Et Me O Ph CH₂C(Me)₂ OEt (R)- V-813 Me Me Me O Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-814 Me Me Me O Ph CH₂C(Me)₂ (CH₂)₂COOH (R)- V-815 Me Et Me O Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-816 Me Et Me O Ph CH₂C(Me)₂ (CH₂)₂COOH (R)- V-817 Me Me Me NH Ph CH₂ Me racemic V-818 Me Me Me NH Ph CH₂ Me (S)- V-819 Me Et Me NH Ph CH₂ Me racemic V-820 Me Et Me NH Ph CH₂ Me (S)- V-821 Me Me Me NH Ph CH₂ Et racemic V-822 Me Me Me NH Ph CH₂ Et (S)- V-823 Me Et Me NH Ph CH₂ Et racemic V-824 Me Et Me NH Ph CH₂ Et (S)- V-825 Me Me Me NH Ph CH₂ nPr racemic

TABLE 118 (Vb)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-826 Me Me Me NH Ph CH₂ nPr (S)- V-827 Me Et Me NH Ph CH₂ nPr racemic V-828 Me Et Me NH Ph CH₂ nPr (S)- V-829 Me Me Me NH Ph CH₂ iPr racemic V-830 Me Me Me NH Ph CH₂ iPr (S)- V-831 Me Et Me NH Ph CH₂ iPr racemic V-832 Me Et Me NH Ph CH₂ iPr (S)- V-833 Me Me Me NH Ph CH₂ nBu racemic V-834 Me Me Me NH Ph CH₂ nBu (S)- V-835 Me Et Me NH Ph CH₂ nBu racemic V-836 Me Et Me NH Ph CH₂ nBu (S)- V-837 Me Me Me NH Ph CH₂ tBu racemic V-838 Me Me Me NH Ph CH₂ tBu (S)- V-839 Me Et Me NH Ph CH₂ tBu racemic V-840 Me Et Me NH Ph CH₂ tBu (S)- V-841 Me Me Me NH Ph CH₂ iBu racemic V-842 Me Me Me NH Ph CH₂ iBu (S)- V-843 Me Et Me NH Ph CH₂ iBu racemic V-844 Me Et Me NH Ph CH₂ iBu (S)- V-845 Me Me Me NH Ph CH₂ n-Heptyl racemic V-846 Me Me Me NH Ph CH₂ n-Heptyl (S)- V-847 Me Et Me NH Ph CH₂ n-Heptyl racemic V-848 Me Et Me NH Ph CH₂ n-Heptyl (S)- V-849 Me Me Me NH Ph CH₂ n-Undecyl racemic V-850 Me Me Me NH Ph CH₂ n-Undecyl (S)- V-851 Me Et Me NH Ph CH₂ n-Undecyl racemic V-852 Me Et Me NH Ph CH₂ n-Undecyl (S)- V-853 Me Me Me NH Ph CH₂ Ph racemic V-854 Me Me Me NH Ph CH₂ Ph (S)- V-855 Me Et Me NH Ph CH₂ Ph racemic V-856 Me Et Me NH Ph CH₂ Ph (S)- V-857 Me Me Me NH Ph CH₂ OEt racemic V-858 Me Me Me NH Ph CH₂ OEt (S)- V-859 Me Et Me NH Ph CH₂ OEt racemic V-860 Me Et Me NH Ph CH₂ OEt (S)- V-861 Me Me Me NH Ph CH₂ (CH₂)₂COOH  racemic V-862 Me Me Me NH Ph CH₂ (CH₂)₂COOH (S)- V-863 Me Et Me NH Ph CH₂ (CH₂)₂COOH racemic V-864 Me Et Me NH Ph CH₂ (CH₂)₂COOH (S)- V-865 Me Me Me NH Ph C(Me)₂ Me racemic V-866 Me Me Me NH Ph C(Me)₂ Me (S)- V-867 Me Et Me NH Ph C(Me)₂ Me racemic V-868 Me Et Me NH Ph C(Me)₂ Me (S)- V-869 Me Me Me NH Ph C(Me)₂ Et racemic V-870 Me Me Me NH Ph C(Me)₂ Et (S)- V-871 Me Et Me NH Ph C(Me)₂ Et racemic V-872 Me Et Me NH Ph C(Me)₂ Et (S)- V-873 Me Me Me NH Ph C(Me)₂ nPr racemic V-874 Me Me Me NH Ph C(Me)₂ nPr (S)- V-875 Me Et Me NH Ph C(Me)₂ nPr racemic

TABLE 119 (Vb)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-876 Me Et Me NH Ph C(Me)₂ nPr (S)- V-877 Me Me Me NH Ph C(Me)₂ iPr racemic V-878 Me Me Me NH Ph C(Me)₂ iPr (S)- V-879 Me Et Me NH Ph C(Me)₂ iPr racemic V-880 Me Et Me NH Ph C(Me)₂ iPr (S)- V-881 Me Me Me NH Ph C(Me)₂ nBu racemic V-882 Me Me Me NH Ph C(Me)₂ nBu (S)- V-883 Me Et Me NH Ph C(Me)₂ nBu racemic V-884 Me Et Me NH Ph C(Me)₂ nBu (S)- V-885 Me Me Me NH Ph C(Me)₂ tBu racemic V-886 Me Me Me NH Ph C(Me)₂ tBu (S)- V-887 Me Et Me NH Ph C(Me)₂ tBu racemic V-888 Me Et Me NH Ph C(Me)₂ tBu (S)- V-889 Me Me Me NH Ph C(Me)₂ iBu racemic V-890 Me Me Me NH Ph C(Me)₂ iBu (S)- V-891 Me Et Me NH Ph C(Me)₂ iBu racemic V-892 Me Et Me NH Ph C(Me)₂ iBu (S)- V-893 Me Me Me NH Ph C(Me)₂ n-Heptyl racemic V-894 Me Me Me NH Ph C(Me)₂ n-Heptyl (S)- V-895 Me Et Me NH Ph C(Me)₂ n-Heptyl racemic V-896 Me Et Me NH Ph C(Me)₂ n-Heptyl (S)- V-897 Me Me Me NH Ph C(Me)₂ n-Undecyl racemic V-898 Me Me Me NH Ph C(Me)₂ n-Undecyl (S)- V-899 Me Et Me NH Ph C(Me)₂ n-Undecyl racemic V-900 Me Et Me NH Ph C(Me)₂ n-Undecyl (S)- V-901 Me Me Me NH Ph C(Me)₂ Ph racemic V-902 Me Me Me NH Ph C(Me)₂ Ph (S)- V-903 Me Et Me NH Ph C(Me)₂ Ph racemic V-904 Me Et Me NH Ph C(Me)₂ Ph (S)- V-905 Me Me Me NH Ph C(Me)₂ OEt racemic V-906 Me Me Me NH Ph C(Me)₂ OEt (S)- V-907 Me Et Me NH Ph C(Me)₂ OEt racemic V-908 Me Et Me NH Ph C(Me)₂ OEt (S)- V-909 Me Me Me NH Ph C(Me)₂ (CH₂)₂COOH  racemic V-910 Me Me Me NH Ph C(Me)₂ (CH₂)₂COOH (S)- V-911 Me Et Me NH Ph C(Me)₂ (CH₂)₂COOH racemic V-912 Me Et Me NH Ph C(Me)₂ (CH₂)₂COOH (S)- V-913 Me Me Me NH Ph (CH₂)₂ Me racemic V-914 Me Me Me NH Ph (CH₂)₂ Me (R)- V-915 Me Et Me NH Ph (CH₂)₂ Me racemic V-916 Me Et Me NH Ph (CH₂)₂ Me (R)- V-917 Me Me Me NH Ph (CH₂)₂ Et racemic V-918 Me Me Me NH Ph (CH₂)₂ Et (R)- V-919 Me Et Me NH Ph (CH₂)₂ Et racemic V-920 Me Et Me NH Ph (CH₂)₂ Et (R)- V-921 Me Me Me NH Ph (CH₂)₂ nPr racemic V-922 Me Me Me NH Ph (CH₂)₂ nPr (R)- V-923 Me Et Me NH Ph (CH₂)₂ nPr racemic V-924 Me Et Me NH Ph (CH₂)₂ nPr (R)- V-925 Me Me Me NH Ph (CH₂)₂ iPr racemic

TABLE 120 (Vb)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-926 Me Me Me NH Ph (CH₂)₂ iPr (R)- V-927 Me Et Me NH Ph (CH₂)₂ iPr racemic V-928 Me Et Me NH Ph (CH₂)₂ iPr (R)- V-929 Me Me Me NH Ph (CH₂)₂ nBu racemic V-930 Me Me Me NH Ph (CH₂)₂ nBu (R)- V-931 Me Et Me NH Ph (CH₂)₂ nBu racemic V-932 Me Et Me NH Ph (CH₂)₂ nBu (R)- V-933 Me Me Me NH Ph (CH₂)₂ tBu racemic V-934 Me Me Me NH Ph (CH₂)₂ tBu (R)- V-935 Me Et Me NH Ph (CH₂)₂ tBu racemic V-936 Me Et Me NH Ph (CH₂)₂ tBu (R)- V-937 Me Me Me NH Ph (CH₂)₂ iBu racemic V-938 Me Me Me NH Ph (CH₂)₂ iBu (R)- V-939 Me Et Me NH Ph (CH₂)₂ iBu racemic V-940 Me Et Me NH Ph (CH₂)₂ iBu (R)- V-941 Me Me Me NH Ph (CH₂)₂ n-Heptyl racemic V-942 Me Me Me NH Ph (CH₂)₂ n-Heptyl (R)- V-943 Me Et Me NH Ph (CH₂)₂ n-Heptyl racemic V-944 Me Et Me NH Ph (CH₂)₂ n-Heptyl (R)- V-945 Me Me Me NH Ph (CH₂)₂ n-Undecyl racemic V-946 Me Me Me NH Ph (CH₂)₂ n-Undecyl (R)- V-947 Me Et Me NH Ph (CH₂)₂ n-Undecyl racemic V-948 Me Et Me NH Ph (CH₂)₂ n-Undecyl (R)- V-949 Me Me Me NH Ph (CH₂)₂ Ph racemic V-950 Me Me Me NH Ph (CH₂)₂ Ph (R)- V-951 Me Et Me NH Ph (CH₂)₂ Ph racemic V-952 Me Et Me NH Ph (CH₂)₂ Ph (R)- V-953 Me Me Me NH Ph (CH₂)₂ OEt racemic V-954 Me Me Me NH Ph (CH₂)₂ OEt (R)- V-955 Me Et Me NH Ph (CH₂)₂ OEt racemic V-956 Me Et Me NH Ph (CH₂)₂ OEt (R)- V-957 Me Me Me NH Ph (CH₂)₂ (CH₂)₂COOH racemic V-958 Me Me Me NH Ph (CH₂)₂ (CH₂)₂COOH (R)- V-959 Me Et Me NH Ph (CH₂)₂ (CH₂)₂COOH racemic V-960 Me Et Me NH Ph (CH₂)₂ (CH₂)₂COOH (R)- V-961 Me Me Me NH Ph CH₂C(Me)₂ Me racemic V-962 Me Me Me NH Ph CH₂C(Me)₂ Me (R)- V-963 Me Et Me NH Ph CH₂C(Me)₂ Me racemic V-964 Me Et Me NH Ph CH₂C(Me)₂ Me (R)- V-965 Me Me Me NH Ph CH₂C(Me)₂ Et racemic V-966 Me Me Me NH Ph CH₂C(Me)₂ Et (R)- V-967 Me Et Me NH Ph CH₂C(Me)₂ Et racemic V-968 Me Et Me NH Ph CH₂C(Me)₂ Et (R)- V-969 Me Me Me NH Ph CH₂C(Me)₂ nPr racemic V-970 Me Me Me NH Ph CH₂C(Me)₂ nPr (R)- V-971 Me Et Me NH Ph CH₂C(Me)₂ nPr racemic V-972 Me Et Me NH Ph CH₂C(Me)₂ nPr (R)- V-973 Me Me Me NH Ph CH₂C(Me)₂ iPr racemic V-974 Me Me Me NH Ph CH₂C(Me)₂ iPr (R)- V-975 Me Et Me NH Ph CH₂C(Me)₂ iPr racemic

TABLE 121 (Vb)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-976 Me Et Me NH Ph CH₂C(Me)₂ iPr (R)- V-977 Me Me Me NH Ph CH₂C(Me)₂ nBu racemic V-978 Me Me Me NH Ph CH₂C(Me)₂ nBu (R)- V-979 Me Et Me NH Ph CH₂C(Me)₂ nBu racemic V-980 Me Et Me NH Ph CH₂C(Me)₂ nBu (R)- V-981 Me Me Me NH Ph CH₂C(Me)₂ tBu racemic V-982 Me Me Me NH Ph CH₂C(Me)₂ tBu (R)- V-983 Me Et Me NH Ph CH₂C(Me)₂ tBu racemic V-984 Me Et Me NH Ph CH₂C(Me)₂ tBu (R)- V-985 Me Me Me NH Ph CH₂C(Me)₂ iBu racemic V-986 Me Me Me NH Ph CH₂C(Me)₂ iBu (R)- V-987 Me Et Me NH Ph CH₂C(Me)₂ iBu racemic V-988 Me Et Me NH Ph CH₂C(Me)₂ iBu (R)- V-989 Me Me Me NH Ph CH₂C(Me)₂ n-Heptyl racemic V-990 Me Me Me NH Ph CH₂C(Me)₂ n-Heptyl (R)- V-991 Me Et Me NH Ph CH₂C(Me)₂ n-Heptyl racemic V-992 Me Et Me NH Ph CH₂C(Me)₂ n-Heptyl (R)- V-993 Me Me Me NH Ph CH₂C(Me)₂ n-Undecyl racemic V-994 Me Me Me NH Ph CH₂C(Me)₂ n-Undecyl (R)- V-995 Me Et Me NH Ph CH₂C(Me)₂ n-Undecyl racemic V-996 Me Et Me NH Ph CH₂C(Me)₂ n-Undecyl (R)- V-997 Me Me Me NH Ph CH₂C(Me)₂ Ph racemic V-998 Me Me Me NH Ph CH₂C(Me)₂ Ph (R)- V-999 Me Et Me NH Ph CH₂C(Me)₂ Ph racemic V-1000 Me Et Me NH Ph CH₂C(Me)₂ Ph (R)- V-1001 Me Me Me NH Ph CH₂C(Me)₂ OEt racemic V-1002 Me Me Me NH Ph CH₂C(Me)₂ OEt (R)- V-1003 Me Et Me NH Ph CH₂C(Me)₂ OEt racemic V-1004 Me Et Me NH Ph CH₂C(Me)₂ OEt (R)- V-1005 Me Me Me NH Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-1006 Me Me Me NH Ph CH₂C(Me)₂ (CH₂)₂COOH (R)- V-1007 Me Et Me NH Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-1008 Me Et Me NH Ph CH₂C(Me)₂ (CH₂)₂COOH (R)- V-1009 Me Me Me CH₂ Ph CH₂ Me racemic V-1010 Me Me Me CH₂ Ph CH₂ Me (S)- V-1011 Me Et Me CH₂ Ph CH₂ Me racemic V-1012 Me Et Me CH₂ Ph CH₂ Me (S)- V-1013 Me Me Me CH₂ Ph CH₂ Et racemic V-1014 Me Me Me CH₂ Ph CH₂ Et (S)- V-1015 Me Et Me CH₂ Ph CH₂ Et racemic V-1016 Me Et Me CH₂ Ph CH₂ Et (S)- V-1017 Me Me Me CH₂ Ph CH₂ nPr racemic V-1018 Me Me Me CH₂ Ph CH₂ nPr (S)- V-1019 Me Et Me CH₂ Ph CH₂ nPr racemic V-1020 Me Et Me CH₂ Ph CH₂ nPr (S)- V-1021 Me Me Me CH₂ Ph CH₂ iPr racemic V-1022 Me Me Me CH₂ Ph CH₂ iPr (S)- V-1023 Me Et Me CH₂ Ph CH₂ iPr racemic V-1024 Me Et Me CH₂ Ph CH₂ iPr (S)- V-1025 Me Me Me CH₂ Ph CH₂ nBu racemic

TABLE 122 (Vb)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-1026 Me Me Me CH₂ Ph CH₂ nBu (S)- V-1027 Me Et Me CH₂ Ph CH₂ nBu racemic V-1028 Me Et Me CH₂ Ph CH₂ nBu (S)- V-1029 Me Me Me CH₂ Ph CH₂ tBu racemic V-1030 Me Me Me CH₂ Ph CH₂ tBu (S)- V-1031 Me Et Me CH₂ Ph CH₂ tBu racemic V-1032 Me Et Me CH₂ Ph CH₂ tBu (S)- V-1033 Me Me Me CH₂ Ph CH₂ iBu racemic V-1034 Me Me Me CH₂ Ph CH₂ iBu (S)- V-1035 Me Et Me CH₂ Ph CH₂ iBu racemic V-1036 Me Et Me CH₂ Ph CH₂ iBu (S)- V-1037 Me Me Me CH₂ Ph CH₂ n-Heptyl racemic V-1038 Me Me Me CH₂ Ph CH₂ n-Heptyl (S)- V-1039 Me Et Me CH₂ Ph CH₂ n-Heptyl racemic V-1040 Me Et Me CH₂ Ph CH₂ n-Heptyl (S)- V-1041 Me Me Me CH₂ Ph CH₂ n-Undecyl racemic V-1042 Me Me Me CH₂ Ph CH₂ n-Undecyl (S)- V-1043 Me Et Me CH₂ Ph CH₂ n-Undecyl racemic V-1044 Me Et Me CH₂ Ph CH₂ n-Undecyl (S)- V-1045 Me Me Me CH₂ Ph CH₂ Ph racemic V-1046 Me Me Me CH₂ Ph CH₂ Ph (S)- V-1047 Me Et Me CH₂ Ph CH₂ Ph racemic V-1048 Me Et Me CH₂ Ph CH₂ Ph (S)- V-1049 Me Me Me CH₂ Ph CH₂ OEt racemic V-1050 Me Me Me CH₂ Ph CH₂ OEt (S)- V-1051 Me Et Me CH₂ Ph CH₂ OEt racemic V-1052 Me Et Me CH₂ Ph CH₂ OEt (S)- V-1053 Me Me Me CH₂ Ph CH₂ (CH₂)₂COOH racemic V-1054 Me Me Me CH₂ Ph CH₂ (CH₂)₂COOH (S)- V-1055 Me Et Me CH₂ Ph CH₂ (CH₂)₂COOH racemic V-1056 Me Et Me CH₂ Ph CH₂ (CH₂)₂COOH (S)- V-1057 Me Me Me CH₂ Ph — Me racemic V-1058 Me Me Me CH₂ Ph — Me (S)- V-1059 Me Et Me CH₂ Ph — Me racemic V-1060 Me Et Me CH₂ Ph — Me (S)- V-1061 Me Me Me CH₂ Ph — Et racemic V-1062 Me Me Me CH₂ Ph — Et (S)- V-1063 Me Et Me CH₂ Ph — Et racemic V-1064 Me Et Me CH₂ Ph — Et (S)- V-1065 Me Me Me CH₂ Ph — nPr racemic V-1066 Me Me Me CH₂ Ph — nPr (S)- V-1067 Me Et Me CH₂ Ph — nPr racemic V-1068 Me Et Me CH₂ Ph — nPr (S)- V-1069 Me Me Me CH₂ Ph — iPr racemic V-1070 Me Me Me CH₂ Ph — iPr (S)- V-1071 Me Et Me CH₂ Ph — iPr racemic V-1072 Me Et Me CH₂ Ph — iPr (S)- V-1073 Me Me Me CH₂ Ph — nBu racemic V-1074 Me Me Me CH₂ Ph — nBu (S)- V-1075 Me Et Me CH₂ Ph — nBu racemic

TABLE 123 (Vb)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-1076 Me Et Me CH₂ Ph — nBu (S)- V-1077 Me Me Me CH₂ Ph — tBu racemic V-1078 Me Me Me CH₂ Ph — tBu (S)- V-1079 Me Et Me CH₂ Ph — tBu racemic V-1080 Me Et Me CH₂ Ph — tBu (S)- V-1081 Me Me Me CH₂ Ph — iBu racemic V-1082 Me Me Me CH₂ Ph — iBu (S)- V-1083 Me Et Me CH₂ Ph — iBu racemic V-1084 Me Et Me CH₂ Ph — iBu (S)- V-1085 Me Me Me CH₂ Ph — n-Heptyl racemic V-1086 Me Me Me CH₂ Ph — n-Heptyl (S)- V-1087 Me Et Me CH₂ Ph — n-Heptyl racemic V-1088 Me Et Me CH₂ Ph — n-Heptyl (S)- V-1089 Me Me Me CH₂ Ph — n-Undecyl racemic V-1090 Me Me Me CH₂ Ph — n-Undecyl (S)- V-1091 Me Et Me CH₂ Ph — n-Undecyl racemic V-1092 Me Et Me CH₂ Ph — n-Undecyl (S)- V-1093 Me Me Me CH₂ Ph — Ph racemic V-1094 Me Me Me CH₂ Ph — Ph (S)- V-1095 Me Et Me CH₂ Ph — Ph racemic V-1096 Me Et Me CH₂ Ph — Ph (S)- V-1097 Me Me Me CH₂ Ph — OEt racemic V-1098 Me Me Me CH₂ Ph — OEt (S)- V-1099 Me Et Me CH₂ Ph — OEt racemic V-1100 Me Et Me CH₂ Ph — OEt (S)- V-1101 Me Me Me CH₂ Ph — (CH₂)₂COOH racemic V-1102 Me Me Me CH₂ Ph — (CH₂)₂COOH (S)- V-1103 Me Et Me CH₂ Ph — (CH₂)₂COOH racemic V-1104 Me Et Me CH₂ Ph — (CH₂)₂COOH (S)- V-1105 Me Me Me CH₂ Ph C(Me)₂ Me racemic V-1106 Me Me Me CH₂ Ph C(Me)₂ Me (S)- V-1107 Me Et Me CH₂ Ph C(Me)₂ Me racemic V-1108 Me Et Me CH₂ Ph C(Me)₂ Me (S)- V-1109 Me Me Me CH₂ Ph C(Me)₂ Et racemic V-1110 Me Me Me CH₂ Ph C(Me)₂ Et (S)- V-1111 Me Et Me CH₂ Ph C(Me)₂ Et racemic V-1112 Me Et Me CH₂ Ph C(Me)₂ Et (S)- V-1113 Me Me Me CH₂ Ph C(Me)₂ nPr racemic V-1114 Me Me Me CH₂ Ph C(Me)₂ nPr (S)- V-1115 Me Et Me CH₂ Ph C(Me)₂ nPr racemic V-1116 Me Et Me CH₂ Ph C(Me)₂ nPr (S)- V-1117 Me Me Me CH₂ Ph C(Me)₂ iPr racemic V-1118 Me Me Me CH₂ Ph C(Me)₂ iPr (S)- V-1119 Me Et Me CH₂ Ph C(Me)₂ iPr racemic V-1120 Me Et Me CH₂ Ph C(Me)₂ iPr (S)- V-1121 Me Me Me CH₂ Ph C(Me)₂ nBu racemic V-1122 Me Me Me CH₂ Ph C(Me)₂ nBu (S)- V-1123 Me Et Me CH₂ Ph C(Me)₂ nBu racemic V-1124 Me Et Me CH₂ Ph C(Me)₂ nBu (S)- V-1125 Me Me Me CH₂ Ph C(Me)₂ tBu racemic

TABLE 124 (Vb)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁶ figuration V-1126 Me Me Me CH₂ Ph C(Me)₂ tBu (S)- V-1127 Me Et Me CH₂ Ph C(Me)₂ tBu racemic V-1128 Me Et Me CH₂ Ph C(Me)₂ tBu (S)- V-1129 Me Me Me CH₂ Ph C(Me)₂ iBu racemic V-1130 Me Me Me CH₂ Ph C(Me)₂ iBu (S)- V-1131 Me Et Me CH₂ Ph C(Me)₂ iBu racemic V-1132 Me Et Me CH₂ Ph C(Me)₂ iBu (S)- V-1133 Me Me Me CH₂ Ph C(Me)₂ n-Heptyl racemic V-1134 Me Me Me CH₂ Ph C(Me)₂ n-Heptyl (S)- V-1135 Me Et Me CH₂ Ph C(Me)₂ n-Heptyl racemic V-1136 Me Et Me CH₂ Ph C(Me)₂ n-Heptyl (S)- V-1137 Me Me Me CH₂ Ph C(Me)₂ n-Undecyl racemic V-1138 Me Me Me CH₂ Ph C(Me)₂ n-Undecyl (S)- V-1139 Me Et Me CH₂ Ph C(Me)₂ n-Undecyl racemic V-1140 Me Et Me CH₂ Ph C(Me)₂ n-Undecyl (S)- V-1141 Me Me Me CH₂ Ph C(Me)₂ Ph racemic V-1142 Me Me Me CH₂ Ph C(Me)₂ Ph (S)- V-1143 Me Et Me CH₂ Ph C(Me)₂ Ph racemic V-1144 Me Et Me CH₂ Ph C(Me)₂ Ph (S)- V-1145 Me Me Me CH₂ Ph C(Me)₂ OEt racemic V-1146 Me Me Me CH₂ Ph C(Me)₂ OEt (S)- V-1147 Me Et Me CH₂ Ph C(Me)₂ OEt racemic V-1148 Me Et Me CH₂ Ph C(Me)₂ OEt (S)- V-1149 Me Me Me CH₂ Ph C(Me)₂ (CH₂)₂COOH racemic V-1150 Me Me Me CH₂ Ph C(Me)₂ (CH₂)₂COOH (S)- V-1151 Me Et Me CH₂ Ph C(Me)₂ (CH₂)₂COOH racemic V-1152 Me Et Me CH₂ Ph C(Me)₂ (CH₂)₂COOH (S)- V-1153 Me Me Me CH₂ Ph (CH₂)₂ Me racemic V-1154 Me Me Me CH₂ Ph (CH₂)₂ Me (S)- V-1155 Me Et Me CH₂ Ph (CH₂)₂ Me racemic V-1156 Me Et Me CH₂ Ph (CH₂)₂ Me (S)- V-1157 Me Me Me CH₂ Ph (CH₂)₂ Et racemic V-1158 Me Me Me CH₂ Ph (CH₂)₂ Et (S)- V-1159 Me Et Me CH₂ Ph (CH₂)₂ Et racemic V-1160 Me Et Me CH₂ Ph (CH₂)₂ Et (S)- V-1161 Me Me Me CH₂ Ph (CH₂)₂ nPr racemic V-1162 Me Me Me CH₂ Ph (CH₂)₂ nPr (S)- V-1163 Me Et Me CH₂ Ph (CH₂)₂ nPr racemic V-1164 Me Et Me CH₂ Ph (CH₂)₂ nPr (S)- V-1165 Me Me Me CH₂ Ph (CH₂)₂ iPr racemic V-1166 Me Me Me CH₂ Ph (CH₂)₂ iPr (S)- V-1167 Me Et Me CH₂ Ph (CH₂)₂ iPr racemic V-1168 Me Et Me CH₂ Ph (CH₂)₂ iPr (S)- V-1169 Me Me Me CH₂ Ph (CH₂)₂ nBu racemic V-1170 Me Me Me CH₂ Ph (CH₂)₂ nBu (S)- V-1171 Me Et Me CH₂ Ph (CH₂)₂ nBu racemic V-1172 Me Et Me CH₂ Ph (CH₂)₂ nBu (S)- V-1173 Me Me Me CH₂ Ph (CH₂)₂ tBu racemic V-1174 Me Me Me CH₂ Ph (CH₂)₂ tBu (S)- V-1175 Me Et Me CH₂ Ph (CH₂)₂ tBu racemic

TABLE 125 (Vb)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-1176 Me Et Me CH₂ Ph (CH₂)₂ tBu (S)- V-1177 Me Me Me CH₂ Ph (CH₂)₂ iBu racemic V-1178 Me Me Me CH₂ Ph (CH₂)₂ iBu (S)- V-1179 Me Et Me CH₂ Ph (CH₂)₂ iBu racemic V-1180 Me Et Me CH₂ Ph (CH₂)₂ iBu (S)- V-1181 Me Me Me CH₂ Ph (CH₂)₂ n-Heptyl racemic V-1182 Me Me Me CH₂ Ph (CH₂)₂ n-Heptyl (S)- V-1183 Me Et Me CH₂ Ph (CH₂)₂ n-Heptyl racemic V-1184 Me Et Me CH₂ Ph (CH₂)₂ n-Heptyl (S)- V-1185 Me Me Me CH₂ Ph (CH₂)₂ n-Undecyl racemic V-1186 Me Me Me CH₂ Ph (CH₂)₂ n-Undecyl (S)- V-1187 Me Et Me CH₂ Ph (CH₂)₂ n-Undecyl racemic V-1188 Me Et Me CH₂ Ph (CH₂)₂ n-Undecyl (S)- V-1189 Me Me Me CH₂ Ph (CH₂)₂ Ph racemic V-1190 Me Me Me CH₂ Ph (CH₂)₂ Ph (S)- V-1191 Me Et Me CH₂ Ph (CH₂)₂ Ph racemic V-1192 Me Et Me CH₂ Ph (CH₂)₂ Ph (S)- V-1193 Me Me Me CH₂ Ph (CH₂)₂ OEt racemic V-1194 Me Me Me CH₂ Ph (CH₂)₂ OEt (S)- V-1195 Me Et Me CH₂ Ph (CH₂)₂ OEt racemic V-1196 Me Et Me CH₂ Ph (CH₂)₂ OEt (S)- V-1197 Me Me Me CH₂ Ph (CH₂)₂ (CH₂)₂COOH racemic V-1198 Me Me Me CH₂ Ph (CH₂)₂ (CH₂)₂COOH (S)- V-1199 Me Et Me CH₂ Ph (CH₂)₂ (CH₂)₂COOH racemic V-1200 Me Et Me CH₂ Ph (CH₂)₂ (CH₂)₂COOH (S)- V-1201 Me Me Me CH₂ Ph CH₂C(Me)₂ Me racemic V-1202 Me Me Me CH₂ Ph CH₂C(Me)₂ Me (S)- V-1203 Me Et Me CH₂ Ph CH₂C(Me)₂ Me racemic V-1204 Me Et Me CH₂ Ph CH₂C(Me)₂ Me (S)- V-1205 Me Me Me CH₂ Ph CH₂C(Me)₂ Et racemic V-1206 Me Me Me CH₂ Ph CH₂C(Me)₂ Et (S)- V-1207 Me Et Me CH₂ Ph CH₂C(Me)₂ Et racemic V-1208 Me Et Me CH₂ Ph CH₂C(Me)₂ Et (S)- V-1209 Me Me Me CH₂ Ph CH₂C(Me)₂ nPr racemic V-1210 Me Me Me CH₂ Ph CH₂C(Me)₂ nPr (S)- V-1211 Me Et Me CH₂ Ph CH₂C(Me)₂ nPr racemic V-1212 Me Et Me CH₂ Ph CH₂C(Me)₂ nPr (S)- V-1213 Me Me Me CH₂ Ph CH₂C(Me)₂ iPr racemic V-1214 Me Me Me CH₂ Ph CH₂C(Me)₂ iPr (S)- V-1215 Me Et Me CH₂ Ph CH₂C(Me)₂ iPr racemic V-1216 Me Et Me CH₂ Ph CH₂C(Me)₂ iPr (S)- V-1217 Me Me Me CH₂ Ph CH₂C(Me)₂ nBu racemic V-1218 Me Me Me CH₂ Ph CH₂C(Me)₂ nBu (S)- V-1219 Me Et Me CH₂ Ph CH₂C(Me)₂ nBu racemic V-1220 Me Et Me CH₂ Ph CH₂C(Me)₂ nBu (S)- V-1221 Me Me Me CH₂ Ph CH₂C(Me)₂ tBu racemic V-1222 Me Me Me CH₂ Ph CH₂C(Me)₂ tBu (S)- V-1223 Me Et Me CH₂ Ph CH₂C(Me)₂ tBu racemic V-1224 Me Et Me CH₂ Ph CH₂C(Me)₂ tBu (S)- V-1225 Me Me Me CH₂ Ph CH₂C(Me)₂ iBu racemic

TABLE 126 (Vb)

Com- Con- pound figura- No. R¹ R² R³ L² R⁴ L³ R⁶ tion V-1226 Me Me Me CH₂ Ph CH₂C(Me)₂ iBu (S)- V-1227 Me Et Me CH₂ Ph CH₂C(Me)₂ iBu racemic V-1228 Me Et Me CH₂ Ph CH₂C(Me)₂ iBu (S)- V-1229 Me Me Me CH₂ Ph CH₂C(Me)₂ n-Heptyl racemic V-1230 Me Me Me CH₂ Ph CH₂C(Me)₂ n-Heptyl (S)- V-1231 Me Et Me CH₂ Ph CH₂C(Me)₂ n-Heptyl racemic V-1232 Me Et Me CH₂ Ph CH₂C(Me)₂ n-Heptyl (S)- V-1233 Me Me Me CH₂ Ph CH₂C(Me)₂ n-Undecyl racemic V-1234 Me Me Me CH₂ Ph CH₂C(Me)₂ n-Undecyl (S)- V-1235 Me Et Me CH₂ Ph CH₂C(Me)₂ n-Undecyl racemic V-1236 Me Et Me CH₂ Ph CH₂C(Me)₂ n-Undecyl (S)- V-1237 Me Me Me CH₂ Ph CH₂C(Me)₂ Ph racemic V-1238 Me Me Me CH₂ Ph CH₂C(Me)₂ Ph (S)- V-1239 Me Et Me CH₂ Ph CH₂C(Me)₂ Ph racemic V-1240 Me Et Me CH₂ Ph CH₂C(Me)₂ Ph (S)- V-1241 Me Me Me CH₂ Ph CH₂C(Me)₂ OEt racemic V-1242 Me Me Me CH₂ Ph CH₂C(Me)₂ OEt (S)- V-1243 Me Et Me CH₂ Ph CH₂C(Me)₂ OEt racemic V-1244 Me Et Me CH₂ Ph CH₂C(Me)₂ OEt (S)- V-1245 Me Me Me CH₂ Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-1246 Me Me Me CH₂ Ph CH₂C(Me)₂ (CH₂)₂COOH (S)- V-1247 Me Et Me CH₂ Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-1248 Me Et Me CH₂ Ph CH₂C(Me)₂ (CH₂)₂COOH (S)-

TABLE 127 (Vb)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁶ figuration V-1972 Me Me Me — Ph — Me racemic V-1973 Me Me Me — Ph — Me (R)- V-1974 Me Et Me — Ph — Me racemic V-1975 Me Et Me — Ph — Me (R)- V-1976 Me Me Me — Ph — Et racemic V-1977 Me Me Me — Ph — Et (R)- V-1978 Me Et Me — Ph — Et racemic V-1979 Me Et Me — Ph — Et (R)- V-1980 Me Me Me — Ph — nPr racemic V-1981 Me Me Me — Ph — nPr (R)- V-1982 Me Et Me — Ph — nPr racemic V-1983 Me Et Me — Ph — nPr (R)- V-1984 Me Me Me — Ph — iPr racemic V-1985 Me Me Me — Ph — iPr (R)- V-1986 Me Et Me — Ph — iPr racemic V-1987 Me Et Me — Ph — iPr (R)- V-1988 Me Me Me — Ph — nBu racemic V-1989 Me Me Me — Ph — nBu (R)- V-1990 Me Et Me — Ph — nBu racemic V-1991 Me Et Me — Ph — nBu (R)- V-1992 Me Me Me — Ph — tBu racemic V-1993 Me Me Me — Ph — tBu (R)- V-1994 Me Et Me — Ph — tBu racemic V-1995 Me Et Me — Ph — tBu (R)- V-1996 Me Me Me — Ph — iBu racemic V-1997 Me Me Me — Ph — iBu (R)- V-1998 Me Et Me — Ph — iBu racemic V-1999 Me Et Me — Ph — iBu (R)- V-2000 Me Me Me — Ph — n-Heptyl racemic V-2001 Me Me Me — Ph — n-Heptyl (R)- V-2002 Me Et Me — Ph — n-Heptyl racemic V-2003 Me Et Me — Ph — n-Heptyl (R)- V-2004 Me Me Me — Ph — n-Undecyl racemic V-2005 Me Me Me — Ph — n-Undecyl (R)- V-2006 Me Et Me — Ph — n-Undecyl racemic V-2007 Me Et Me — Ph — n-Undecyl (R)- V-2008 Me Me Me — Ph — OEt racemic V-2009 Me Me Me — Ph — OEt (R)- V-2010 Me Et Me — Ph — OEt racemic V-2011 Me Et Me — Ph — OEt (R)- V-2012 Me Me Me — Ph — (CH₂)₂COONa racemic V-2013 Me Me Me — Ph — (CH₂)₂COONa (R)- V-2014 Me Et Me — Ph — (CH₂)₂COONa racemic V-2015 Me Et Me — Ph — (CH₂)₂COONa (R)- V-2016 Me Me Me — Ph CH₂ Me racemic V-2017 Me Me Me — Ph CH₂ Me (S)- V-2018 Me Et Me — Ph CH₂ Me racemic V-2019 Me Et Me — Ph CH₂ Me (S)- V-2020 Me Me Me — Ph CH₂ Et racemic V-2021 Me Me Me — Ph CH₂ Et (S)-

TABLE 128 (Vb)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁶ figuration V-2022 Me Et Me — Ph CH₂ Et racemic V-2023 Me Et Me — Ph CH₂ Et (S)- V-2024 Me Me Me — Ph CH₂ nPr racemic V-2025 Me Me Me — Ph CH₂ nPr (S)- V-2026 Me Et Me — Ph CH₂ nPr racemic V-2027 Me Et Me — Ph CH₂ nPr (S)- V-2028 Me Me Me — Ph CH₂ iPr racemic V-2029 Me Me Me — Ph CH₂ iPr (S)- V-2030 Me Et Me — Ph CH₂ iPr racemic V-2031 Me Et Me — Ph CH₂ iPr (S)- V-2032 Me Me Me — Ph CH₂ nBu racemic V-2033 Me Me Me — Ph CH₂ nBu (S)- V-2034 Me Et Me — Ph CH₂ nBu racemic V-2035 Me Et Me — Ph CH₂ nBu (S)- V-2036 Me Me Me — Ph CH₂ tBu racemic V-2037 Me Me Me — Ph CH₂ tBu (S)- V-2038 Me Et Me — Ph CH₂ tBu racemic V-2039 Me Et Me — Ph CH₂ tBu (S)- V-2040 Me Me Me — Ph CH₂ iBu racemic V-2041 Me Me Me — Ph CH₂ iBu (S)- V-2042 Me Et Me — Ph CH₂ iBu racemic V-2043 Me Et Me — Ph CH₂ iBu (S)- V-2044 Me Me Me — Ph CH₂ n-Heptyl racemic V-2045 Me Me Me — Ph CH₂ n-Heptyl (S)- V-2046 Me Et Me — Ph CH₂ n-Heptyl racemic V-2047 Me Et Me — Ph CH₂ n-Heptyl (S)- V-2048 Me Me Me — Ph CH₂ n-Undecyl racemic V-2049 Me Me Me — Ph CH₂ n-Undecyl (S)- V-2050 Me Et Me — Ph CH₂ n-Undecyl racemic V-2051 Me Et Me — Ph CH₂ n-Undecyl (S)- V-2052 Me Me Me — Ph CH₂ OEt racemic V-2053 Me Me Me — Ph CH₂ OEt (S)- V-2054 Me Et Me — Ph CH₂ OEt racemic V-2055 Me Et Me — Ph CH₂ OEt (S)- V-2056 Me Me Me — Ph CH₂ (CH₂)₂COONa racemic V-2057 Me Me Me — Ph CH₂ (CH₂)₂COONa (S)- V-2058 Me Et Me — Ph CH₂ (CH₂)₂COONa racemic V-2059 Me Et Me — Ph CH₂ (CH₂)₂COONa (S)-

TABLE 129 (Vc)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁶ figuration V-1249 Me Me Me O Ph CH₂ Me racemic V-1250 Me Me Me O Ph CH₂ Me (S)- V-1251 Me Et Me O Ph CH₂ Me racemic V-1252 Me Et Me O Ph CH₂ Me (S)- V-1253 Me Me Me O Ph CH₂ Et racemic V-1254 Me Me Me O Ph CH₂ Et (S)- V-1255 Me Et Me O Ph CH₂ Et racemic V-1256 Me Et Me O Ph CH₂ Et (S)- V-1257 Me Me Me O Ph CH₂ nPr racemic V-1258 Me Me Me O Ph CH₂ nPr (S)- V-1259 Me Et Me O Ph CH₂ nPr racemic V-1260 Me Et Me O Ph CH₂ nPr (S)- V-1261 Me Me Me O Ph CH₂ iPr racemic V-1262 Me Me Me O Ph CH₂ iPr (S)- V-1263 Me Et Me O Ph CH₂ iPr racemic V-1264 Me Et Me O Ph CH₂ iPr (S)- V-1265 Me Me Me O Ph CH₂ nBu racemic V-1266 Me Me Me O Ph CH₂ nBu (S)- V-1267 Me Et Me O Ph CH₂ nBu racemic V-1268 Me Et Me O Ph CH₂ nBu (S)- V-1269 Me Me Me O Ph CH₂ tBu racemic V-1270 Me Me Me O Ph CH₂ tBu (S)- V-1271 Me Et Me O Ph CH₂ tBu racemic V-1272 Me Et Me O Ph CH₂ tBu (S)- V-1273 Me Me Me O Ph CH₂ iBu racemic V-1274 Me Me Me O Ph CH₂ iBu (S)- V-1275 Me Et Me O Ph CH₂ iBu racemic V-1276 Me Et Me O Ph CH₂ iBu (S)- V-1277 Me Me Me O Ph CH₂ n-Heptyl racemic V-1278 Me Me Me O Ph CH₂ n-Heptyl (S)- V-1279 Me Et Me O Ph CH₂ n-Heptyl racemic V-1280 Me Et Me O Ph CH₂ n-Heptyl (S)- V-1281 Me Me Me O Ph CH₂ n-Undecyl racemic V-1282 Me Me Me O Ph CH₂ n-Undecyl (S)- V-1283 Me Et Me O Ph CH₂ n-Undecyl racemic V-1284 Me Et Me O Ph CH₂ n-Undecyl (S)- V-1285 Me Me Me O Ph CH₂ Ph racemic V-1286 Me Me Me O Ph CH₂ Ph (S)- V-1287 Me Et Me O Ph CH₂ Ph racemic V-1288 Me Et Me O Ph CH₂ Ph (S)- V-1289 Me Me Me O Ph CH₂ OEt racemic V-1290 Me Me Me O Ph CH₂ OEt (S)- V-1291 Me Et Me O Ph CH₂ OEt racemic V-1292 Me Et Me O Ph CH₂ OEt (S)- V-1293 Me Me Me O Ph CH₂ (CH₂)₂COOH racemic V-1294 Me Me Me O Ph CH₂ (CH₂)₂COOH (S)- V-1295 Me Et Me O Ph CH₂ (CH₂)₂COOH racemic V-1296 Me Et Me O Ph CH₂ (CH₂)₂COOH (S)- V-1297 Me Me Me O Ph C(Me)₂ Me racemic V-1298 Me Me Me O Ph C(Me)₂ Me (S)-

TABLE 130 (Vc)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁶ figuration V-1299 Me Et Me O Ph C(Me)₂ Me racemic V-1300 Me Et Me O Ph C(Me)₂ Me (S)- V-1301 Me Me Me O Ph C(Me)₂ Et racemic V-1302 Me Me Me O Ph C(Me)₂ Et (S)- V-1303 Me Et Me O Ph C(Me)₂ Et racemic V-1304 Me Et Me O Ph C(Me)₂ Et (S)- V-1305 Me Me Me O Ph C(Me)₂ nPr racemic V-1306 Me Me Me O Ph C(Me)₂ nPr (S)- V-1307 Me Et Me O Ph C(Me)₂ nPr racemic V-1308 Me Et Me O Ph C(Me)₂ nPr (S)- V-1309 Me Me Me O Ph C(Me)₂ iPr racemic V-1310 Me Me Me O Ph C(Me)₂ iPr (S)- V-1311 Me Et Me O Ph C(Me)₂ iPr racemic V-1312 Me Et Me O Ph C(Me)₂ iPr (S)- V-1313 Me Me Me O Ph C(Me)₂ nBu racemic V-1314 Me Me Me O Ph C(Me)₂ nBu (S)- V-1315 Me Et Me O Ph C(Me)₂ nBu racemic V-1316 Me Et Me O Ph C(Me)₂ nBu (S)- V-1317 Me Me Me O Ph C(Me)₂ tBu racemic V-1318 Me Me Me O Ph C(Me)₂ tBu (S)- V-1319 Me Et Me O Ph C(Me)₂ tBu racemic V-1320 Me Et Me O Ph C(Me)₂ tBu (S)- V-1321 Me Me Me O Ph C(Me)₂ iBu racemic V-1322 Me Me Me O Ph C(Me)₂ iBu (S)- V-1323 Me Et Me O Ph C(Me)₂ iBu racemic V-1324 Me Et Me O Ph C(Me)₂ iBu (S)- V-1325 Me Me Me O Ph C(Me)₂ n-Heptyl racemic V-1326 Me Me Me O Ph C(Me)₂ n-Heptyl (S)- V-1327 Me Et Me O Ph C(Me)₂ n-Heptyl racemic V-1328 Me Et Me O Ph C(Me)₂ n-Heptyl (S)- V-1329 Me Me Me O Ph C(Me)₂ n-Undecyl racemic V-1330 Me Me Me O Ph C(Me)₂ n-Undecyl (S)- V-1331 Me Et Me O Ph C(Me)₂ n-Undecyl racemic V-1332 Me Et Me O Ph C(Me)₂ n-Undecyl (S)- V-1333 Me Me Me O Ph C(Me)₂ Ph racemic V-1334 Me Me Me O Ph C(Me)₂ Ph (S)- V-1335 Me Et Me O Ph C(Me)₂ Ph racemic V-1336 Me Et Me O Ph C(Me)₂ Ph (S)- V-1337 Me Me Me O Ph C(Me)₂ OEt racemic V-1338 Me Me Me O Ph C(Me)₂ OEt (S)- V-1339 Me Et Me O Ph C(Me)₂ OEt racemic V-1340 Me Et Me O Ph C(Me)₂ OEt (S)- V-1341 Me Me Me O Ph C(Me)₂ (CH₂)₂COOH racemic V-1342 Me Me Me O Ph C(Me)₂ (CH₂)₂COOH (S)- V-1343 Me Et Me O Ph C(Me)₂ (CH₂)₂COOH racemic V-1344 Me Et Me O Ph C(Me)₂ (CH₂)₂COOH (S)- V-1345 Me Me Me O Ph (CH₂)₂ Me racemic V-1346 Me Me Me O Ph (CH₂)₂ Me (R)- V-1347 Me Et Me O Ph (CH₂)₂ Me racemic V-1348 Me Et Me O Ph (CH₂)₂ Me (R)-

TABLE 131 (Vc)

Com- pound Con- No. R¹ R² R³ L² R⁴ L³ R⁶ figuration V-1349 Me Me Me O Ph (CH₂)₂ Et racemic V-1350 Me Me Me O Ph (CH₂)₂ Et (R)- V-1351 Me Et Me O Ph (CH₂)₂ Et racemic V-1352 Me Et Me O Ph (CH₂)₂ Et (R)- V-1353 Me Me Me O Ph (CH₂)₂ nPr racemic V-1354 Me Me Me O Ph (CH₂)₂ nPr (R)- V-1355 Me Et Me O Ph (CH₂)₂ nPr racemic V-1356 Me Et Me O Ph (CH₂)₂ nPr (R)- V-1357 Me Me Me O Ph (CH₂)₂ iPr racemic V-1358 Me Me Me O Ph (CH₂)₂ iPr (R)- V-1359 Me Et Me O Ph (CH₂)₂ iPr racemic V-1360 Me Et Me O Ph (CH₂)₂ iPr (R)- V-1361 Me Me Me O Ph (CH₂)₂ nBu racemic V-1362 Me Me Me O Ph (CH₂)₂ nBu (R)- V-1363 Me Et Me O Ph (CH₂)₂ nBu racemic V-1364 Me Et Me O Ph (CH₂)₂ nBu (R)- V-1365 Me Me Me O Ph (CH₂)₂ tBu racemic V-1366 Me Me Me O Ph (CH₂)₂ tBu (R)- V-1367 Me Et Me O Ph (CH₂)₂ tBu racemic V-1368 Me Et Me O Ph (CH₂)₂ tBu (R)- V-1369 Me Me Me O Ph (CH₂)₂ iBu racemic V-1370 Me Me Me O Ph (CH₂)₂ iBu (R)- V-1371 Me Et Me O Ph (CH₂)₂ iBu racemic V-1372 Me Et Me O Ph (CH₂)₂ iBu (R)- V-1373 Me Me Me O Ph (CH₂)₂ n-Heptyl racemic V-1374 Me Me Me O Ph (CH₂)₂ n-Heptyl (R)- V-1375 Me Et Me O Ph (CH₂)₂ n-Heptyl racemic V-1376 Me Et Me O Ph (CH₂)₂ n-Heptyl (R)- V-1377 Me Me Me O Ph (CH₂)₂ n-Undecyl racemic V-1378 Me Me Me O Ph (CH₂)₂ n-Undecyl (R)- V-1379 Me Et Me O Ph (CH₂)₂ n-Undecyl racemic V-1380 Me Et Me O Ph (CH₂)₂ n-Undecyl (R)- V-1381 Me Me Me O Ph (CH₂)₂ Ph racemic V-1382 Me Me Me O Ph (CH₂)₂ Ph (R)- V-1383 Me Et Me O Ph (CH₂)₂ Ph racemic V-1384 Me Et Me O Ph (CH₂)₂ Ph (R)- V-1385 Me Me Me O Ph (CH₂)₂ OEt racemic V-1386 Me Me Me O Ph (CH₂)₂ OEt (R)- V-1387 Me Et Me O Ph (CH₂)₂ OEt racemic V-1388 Me Et Me O Ph (CH₂)₂ OEt (R)- V-1389 Me Me Me O Ph (CH₂)₂ (CH₂)₂COOH racemic V-1390 Me Me Me O Ph (CH₂)₂ (CH₂)₂COOH (R)- V-1391 Me Et Me O Ph (CH₂)₂ (CH₂)₂COOH racemic V-1392 Me Et Me O Ph (CH₂)₂ (CH₂)₂COOH (R)- V-1393 Me Me Me O Ph CH₂C(Me)₂ Me racemic V-1394 Me Me Me O Ph CH₂C(Me)₂ Me (R)- V-1395 Me Et Me O Ph CH₂C(Me)₂ Me racemic V-1396 Me Et Me O Ph CH₂C(Me)₂ Me (R)- V-1397 Me Me Me O Ph CH₂C(Me)₂ Et racemic V-1398 Me Me Me O Ph CH₂C(Me)₂ Et (R)-

TABLE 132 (Vc)

Com- pound Con- No. R¹ R² R³ L² R⁴ L³ R⁶ figuration V-1399 Me Et Me O Ph CH₂C(Me)₂ Et racemic V-1400 Me Et Me O Ph CH₂C(Me)₂ Et (R)- V-1401 Me Me Me O Ph CH₂C(Me)₂ nPr racemic V-1402 Me Me Me O Ph CH₂C(Me)₂ nPr (R)- V-1403 Me Et Me O Ph CH₂C(Me)₂ nPr racemic V-1404 Me Et Me O Ph CH₂C(Me)₂ nPr (R)- V-1405 Me Me Me O Ph CH₂C(Me)₂ iPr racemic V-1406 Me Me Me O Ph CH₂C(Me)₂ iPr (R)- V-1407 Me Et Me O Ph CH₂C(Me)₂ iPr racemic V-1408 Me Et Me O Ph CH₂C(Me)₂ iPr (R)- V-1409 Me Me Me O Ph CH₂C(Me)₂ nBu racemic V-1410 Me Me Me O Ph CH₂C(Me)₂ nBu (R)- V-1411 Me Et Me O Ph CH₂C(Me)₂ nBu racemic V-1412 Me Et Me O Ph CH₂C(Me)₂ nBu (R)- V-1413 Me Me Me O Ph CH₂C(Me)₂ tBu racemic V-1414 Me Me Me O Ph CH₂C(Me)₂ tBu (R)- V-1415 Me Et Me O Ph CH₂C(Me)₂ tBu racemic V-1416 Me Et Me O Ph CH₂C(Me)₂ tBu (R)- V-1417 Me Me Me O Ph CH₂C(Me)₂ iBu racemic V-1418 Me Me Me O Ph CH₂C(Me)₂ iBu (R)- V-1419 Me Et Me O Ph CH₂C(Me)₂ iBu racemic V-1420 Me Et Me O Ph CH₂C(Me)₂ iBu (R)- V-1421 Me Me Me O Ph CH₂C(Me)₂ n-Heptyl racemic V-1422 Me Me Me O Ph CH₂C(Me)₂ n-Heptyl (R)- V-1423 Me Et Me O Ph CH₂C(Me)₂ n-Heptyl racemic V-1424 Me Et Me O Ph CH₂C(Me)₂ n-Heptyl (R)- V-1425 Me Me Me O Ph CH₂C(Me)₂ n-Undecyl racemic V-1426 Me Me Me O Ph CH₂C(Me)₂ n-Undecyl (R)- V-1427 Me Et Me O Ph CH₂C(Me)₂ n-Undecyl racemic V-1428 Me Et Me O Ph CH₂C(Me)₂ n-Undecyl (R)- V-1429 Me Me Me O Ph CH₂C(Me)₂ Ph racemic V-1430 Me Me Me O Ph CH₂C(Me)₂ Ph (R)- V-1431 Me Et Me O Ph CH₂C(Me)₂ Ph racemic V-1432 Me Et Me O Ph CH₂C(Me)₂ Ph (R)- V-1433 Me Me Me O Ph CH₂C(Me)₂ OEt racemic V-1434 Me Me Me O Ph CH₂C(Me)₂ OEt (R)- V-1435 Me Et Me O Ph CH₂C(Me)₂ OEt racemic V-1436 Me Et Me O Ph CH₂C(Me)₂ OEt (R)- V-1437 Me Me Me O Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-1438 Me Me Me O Ph CH₂C(Me)₂ (CH₂)₂COOH (R)- V-1439 Me Et Me O Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-1440 Me Et Me O Ph CH₂C(Me)₂ (CH₂)₂COOH (R)- V-1441 Me Me Me NH Ph CH₂ Me racemic V-1442 Me Me Me NH Ph CH₂ Me (S)- V-1443 Me Et Me NH Ph CH₂ Me racemic V-1444 Me Et Me NH Ph CH₂ Me (S)- V-1445 Me Me Me NH Ph CH₂ Et racemic V-1446 Me Me Me NH Ph CH₂ Et (S)- V-1447 Me Et Me NH Ph CH₂ Et racemic V-1448 Me Et Me NH Ph CH₂ Et (S)-

TABLE 133 (Vc)

Compound Con- No. R¹ R² R³ L² R⁴ L³ R⁶ figuration V-1449 Me Me Me NH Ph CH₂ nPr racemic V-1450 Me Me Me NH Ph CH₂ nPr (S)- V-1451 Me Et Me NH Ph CH₂ nPr racemic V-1452 Me Et Me NH Ph CH₂ nPr (S)- V-1453 Me Me Me NH Ph CH₂ iPr racemic V-1454 Me Me Me NH Ph CH₂ iPr (S)- V-1455 Me Et Me NH Ph CH₂ iPr racemic V-1456 Me Et Me NH Ph CH₂ iPr (S)- V-1457 Me Me Me NH Ph CH₂ nBu racemic V-1458 Me Me Me NH Ph CH₂ nBu (S)- V-1459 Me Et Me NH Ph CH₂ nBu racemic V-1460 Me Et Me NH Ph CH₂ nBu (S)- V-1461 Me Me Me NH Ph CH₂ tBu racemic V-1462 Me Me Me NH Ph CH₂ tBu (S)- V-1463 Me Et Me NH Ph CH₂ tBu racemic V-1464 Me Et Me NH Ph CH₂ tBu (S)- V-1465 Me Me Me NH Ph CH₂ iBu racemic V-1466 Me Me Me NH Ph CH₂ iBu (S)- V-1467 Me Et Me NH Ph CH₂ iBu racemic V-1468 Me Et Me NH Ph CH₂ iBu (S)- V-1469 Me Me Me NH Ph CH₂ n-Heptyl racemic V-1470 Me Me Me NH Ph CH₂ n-Heptyl (S)- V-1471 Me Et Me NH Ph CH₂ n-Heptyl racemic V-1472 Me Et Me NH Ph CH₂ n-Heptyl (S)- V-1473 Me Me Me NH Ph CH₂ n-Undecyl racemic V-1474 Me Me Me NH Ph CH₂ n-Undecyl (S)- V-1475 Me Et Me NH Ph CH₂ n-Undecyl racemic V-1476 Me Et Me NH Ph CH₂ n-Undecyl (S)- V-1477 Me Me Me NH Ph CH₂ n-Pentadecyl racemic V-1478 Me Me Me NH Ph CH₂ n-Pentadecyl (S)- V-1479 Me Et Me NH Ph CH₂ n-Pentadecyl racemic V-1480 Me Et Me NH Ph CH₂ n-Pentadecyl (S)- V-1481 Me Me Me NH Ph CH₂ Ph racemic V-1482 Me Me Me NH Ph CH₂ Ph (S)- V-1483 Me Et Me NH Ph CH₂ Ph racemic V-1484 Me Et Me NH Ph CH₂ Ph (S)- V-1485 Me Me Me NH Ph CH₂ OEt racemic V-1486 Me Me Me NH Ph CH₂ OEt (S)- V-1487 Me Et Me NH Ph CH₂ OEt racemic V-1488 Me Et Me NH Ph CH₂ OEt (S)- V-1489 Me Me Me NH Ph CH₂ (CH₂)₂COOH racemic V-1490 Me Me Me NH Ph CH₂ (CH₂)₂COOH (S)- V-1491 Me Et Me NH Ph CH₂ (CH₂)₂COOH racemic V-1492 Me Et Me NH Ph CH₂ (CH₂)₂COOH (S)- V-1493 Me Me Me NH Ph CH₂ H racemic V-1494 Me Me Me NH Ph CH₂ H (S)- V-1495 Me Et Me NH Ph CH₂ H racemic V-1496 Me Et Me NH Ph CH₂ H (S)- V-1497 Me Me Me NH Ph CH₂ (5-Methyl-2-oxo- racemic 1,3-dioxol-4- yl)methoxy V-1498 Me Me Me NH Ph CH₂ (5-Methyl-2-oxo- (S)- 1,3-dioxol-4- yl)methoxy

TABLE 134 (Vc)

Com- pound Con- No. R¹ R² R³ L² R⁴ L³ R⁶ figuration V-1499 Me Et Me NH Ph CH₂ (5-Methyl-2-oxo- racemic 1,3-dioxol-4-yl) methoxy V-1500 Me Et Me NH Ph CH₂ (5-Methyl-2-oxo- (S)- 1,3-dioxol-4-yl) methoxy V-1501 Me Me Me NH Ph C(Me)₂ Me (S)- V-1502 Me Et Me NH Ph C(Me)₂ Me racemic V-1503 Me Et Me NH Ph C(Me)₂ Me (S)- V-1504 Me Me Me NH Ph C(Me)₂ Et racemic V-1505 Me Me Me NH Ph C(Me)₂ Et (S)- V-1506 Me Et Me NH Ph C(Me)₂ Et racemic V-1507 Me Et Me NH Ph C(Me)₂ Et (S)- V-1508 Me Me Me NH Ph C(Me)₂ nPr racemic V-1509 Me Me Me NH Ph C(Me)₂ nPr (S)- V-1510 Me Et Me NH Ph C(Me)₂ nPr racemic V-1511 Me Et Me NH Ph C(Me)₂ nPr (S)- V-1512 Me Me Me NH Ph C(Me)₂ iPr racemic V-1513 Me Me Me NH Ph C(Me)₂ iPr (S)- V-1514 Me Et Me NH Ph C(Me)₂ iPr racemic V-1515 Me Et Me NH Ph C(Me)₂ iPr (S)- V-1516 Me Me Me NH Ph C(Me)₂ nBu racemic V-1517 Me Me Me NH Ph C(Me)₂ nBu (S)- V-1518 Me Et Me NH Ph C(Me)₂ nBu racemic V-1519 Me Et Me NH Ph C(Me)₂ nBu (S)- V-1520 Me Me Me NH Ph C(Me)₂ tBu racemic V-1521 Me Me Me NH Ph C(Me)₂ tBu (S)- V-1522 Me Et Me NH Ph C(Me)₂ tBu racemic V-1523 Me Et Me NH Ph C(Me)₂ tBu (S)- V-1524 Me Me Me NH Ph C(Me)₂ iBu racemic V-1525 Me Me Me NH Ph C(Me)₂ iBu (S)- V-1526 Me Et Me NH Ph C(Me)₂ iBu racemic V-1527 Me Et Me NH Ph C(Me)₂ iBu (S)- V-1528 Me Me Me NH Ph C(Me)₂ n-Heptyl racemic V-1529 Me Me Me NH Ph C(Me)₂ n-Heptyl (S)- V-1530 Me Et Me NH Ph C(Me)₂ n-Heptyl racemic V-1531 Me Et Me NH Ph C(Me)₂ n-Heptyl (S)- V-1532 Me Me Me NH Ph C(Me)₂ n-Undecyl racemic V-1533 Me Me Me NH Ph C(Me)₂ n-Undecyl (S)- V-1534 Me Et Me NH Ph C(Me)₂ n-Undecyl racemic V-1535 Me Et Me NH Ph C(Me)₂ n-Undecyl (S)- V-1536 Me Me Me NH Ph C(Me)₂ Ph racemic V-1537 Me Me Me NH Ph C(Me)₂ Ph (S)- V-1538 Me Et Me NH Ph C(Me)₂ Ph racemic V-1539 Me Et Me NH Ph C(Me)₂ Ph (S)- V-1540 Me Me Me NH Ph C(Me)₂ OEt racemic V-1541 Me Me Me NH Ph C(Me)₂ OEt (S)- V-1542 Me Et Me NH Ph C(Me)₂ OEt racemic V-1543 Me Et Me NH Ph C(Me)₂ OEt (S)- V-1544 Me Me Me NH Ph C(Me)₂ (CH₂)₂COOH racemic V-1545 Me Me Me NH Ph C(Me)₂ (CH₂)₂COOH (S)- V-1546 Me Et Me NH Ph C(Me)₂ (CH₂)₂COOH racemic V-1547 Me Et Me NH Ph C(Me)₂ (CH₂)₂COOH (S)- V-1548 Me Me Me NH Ph (CH₂)₂ Me racemic

TABLE 135 (Vc)

Com- pound Con- No. R¹ R² R³ L² R⁴ L³ R⁶ figuration V-1549 Me Me Me NH Ph (CH₂)₂ Me (R)- V-1550 Me Et Me NH Ph (CH₂)₂ Me racemic V-1551 Me Et Me NH Ph (CH₂)₂ Me (R)- V-1552 Me Me Me NH Ph (CH₂)₂ Et racemic V-1553 Me Me Me NH Ph (CH₂)₂ Et (R)- V-1554 Me Et Me NH Ph (CH₂)₂ Et racemic V-1555 Me Et Me NH Ph (CH₂)₂ Et (R)- V-1556 Me Me Me NH Ph (CH₂)₂ nPr racemic V-1557 Me Me Me NH Ph (CH₂)₂ nPr (R)- V-1558 Me Et Me NH Ph (CH₂)₂ nPr racemic V-1559 Me Et Me NH Ph (CH₂)₂ nPr (R)- V-1560 Me Me Me NH Ph (CH₂)₂ iPr racemic V-1561 Me Me Me NH Ph (CH₂)₂ iPr (R)- V-1562 Me Et Me NH Ph (CH₂)₂ iPr racemic V-1563 Me Et Me NH Ph (CH₂)₂ iPr (R)- V-1564 Me Me Me NH Ph (CH₂)₂ nBu racemic V-1565 Me Me Me NH Ph (CH₂)₂ nBu (R)- V-1566 Me Et Me NH Ph (CH₂)₂ nBu racemic V-1567 Me Et Me NH Ph (CH₂)₂ nBu (R)- V-1568 Me Me Me NH Ph (CH₂)₂ tBu racemic V-1569 Me Me Me NH Ph (CH₂)₂ tBu (R)- V-1570 Me Et Me NH Ph (CH₂)₂ tBu racemic V-1571 Me Et Me NH Ph (CH₂)₂ tBu (R)- V-1572 Me Me Me NH Ph (CH₂)₂ iBu racemic V-1573 Me Me Me NH Ph (CH₂)₂ iBu (R)- V-1574 Me Et Me NH Ph (CH₂)₂ iBu racemic V-1575 Me Et Me NH Ph (CH₂)₂ iBu (R)- V-1576 Me Me Me NH Ph (CH₂)₂ n-Heptyl racemic V-1577 Me Me Me NH Ph (CH₂)₂ n-Heptyl (R)- V-1578 Me Et Me NH Ph (CH₂)₂ n-Heptyl racemic V-1579 Me Et Me NH Ph (CH₂)₂ n-Heptyl (R)- V-1580 Me Me Me NH Ph (CH₂)₂ n-Undecyl racemic V-1581 Me Me Me NH Ph (CH₂)₂ n-Undecyl (R)- V-1582 Me Et Me NH Ph (CH₂)₂ n-Undecyl racemic V-1583 Me Et Me NH Ph (CH₂)₂ n-Undecyl (R)- V-1584 Me Me Me NH Ph (CH₂)₂ Ph racemic V-1585 Me Me Me NH Ph (CH₂)₂ Ph (R)- V-1586 Me Et Me NH Ph (CH₂)₂ Ph racemic V-1587 Me Et Me NH Ph (CH₂)₂ Ph (R)- V-1588 Me Me Me NH Ph (CH₂)₂ OEt racemic V-1589 Me Me Me NH Ph (CH₂)₂ OEt (R)- V-1590 Me Et Me NH Ph (CH₂)₂ OEt racemic V-1591 Me Et Me NH Ph (CH₂)₂ OEt (R)- V-1592 Me Me Me NH Ph (CH₂)₂ (CH₂)₂COOH racemic V-1593 Me Me Me NH Ph (CH₂)₂ (CH₂)₂COOH (R)- V-1594 Me Et Me NH Ph (CH₂)₂ (CH₂)₂COOH racemic V-1595 Me Et Me NH Ph (CH₂)₂ (CH₂)₂COOH (R)- V-1596 Me Me Me NH Ph CH₂C(Me)₂ Me racemic V-1597 Me Me Me NH Ph CH₂C(Me)₂ Me (R)- V-1598 Me Et Me NH Ph CH₂C(Me)₂ Me racemic

TABLE 136 (Vc)

Com- Con- pound figu- No. R¹ R² R³ L² R⁴ L³ R⁶ ration V-1599 Me Et Me NH Ph CH₂C(Me)₂ Me (R)- V-1600 Me Me Me NH Ph CH₂C(Me)₂ Et racemic V-1601 Me Me Me NH Ph CH₂C(Me)₂ Et (R)- V-1602 Me Et Me NH Ph CH₂C(Me)₂ Et racemic V-1603 Me Et Me NH Ph CH₂C(Me)₂ Et (R)- V-1604 Me Me Me NH Ph CH₂C(Me)₂ nPr racemic V-1605 Me Me Me NH Ph CH₂C(Me)₂ nPr (R)- V-1606 Me Et Me NH Ph CH₂C(Me)₂ nPr racemic V-1607 Me Et Me NH Ph CH₂C(Me)₂ nPr (R)- V-1608 Me Me Me NH Ph CH₂C(Me)₂ iPr racemic V-1609 Me Me Me NH Ph CH₂C(Me)₂ iPr (R)- V-1610 Me Et Me NH Ph CH₂C(Me)₂ iPr racemic V-1611 Me Et Me NH Ph CH₂C(Me)₂ iPr (R)- V-1612 Me Me Me NH Ph CH₂C(Me)₂ nBu racemic V-1613 Me Me Me NH Ph CH₂C(Me)₂ nBu (R)- V-1614 Me Et Me NH Ph CH₂C(Me)₂ nBu racemic V-1615 Me Et Me NH Ph CH₂C(Me)₂ nBu (R)- V-1616 Me Me Me NH Ph CH₂C(Me)₂ tBu racemic V-1617 Me Me Me NH Ph CH₂C(Me)₂ tBu (R)- V-1618 Me Et Me NH Ph CH₂C(Me)₂ tBu racemic V-1619 Me Et Me NH Ph CH₂C(Me)₂ tBu (R)- V-1620 Me Me Me NH Ph CH₂C(Me)₂ iBu racemic V-1621 Me Me Me NH Ph CH₂C(Me)₂ iBu (R)- V-1622 Me Et Me NH Ph CH₂C(Me)₂ iBu racemic V-1623 Me Et Me NH Ph CH₂C(Me)₂ iBu (R)- V-1624 Me Me Me NH Ph CH₂C(Me)₂ n-Heptyl racemic V-1625 Me Me Me NH Ph CH₂C(Me)₂ n-Heptyl (R)- V-1626 Me Et Me NH Ph CH₂C(Me)₂ n-Heptyl racemic V-1627 Me Et Me NH Ph CH₂C(Me)₂ n-Heptyl (R)- V-1628 Me Me Me NH Ph CH₂C(Me)₂ n-Undecyl racemic V-1629 Me Me Me NH Ph CH₂C(Me)₂ n-Undecyl (R)- V-1630 Me Et Me NH Ph CH₂C(Me)₂ n-Undecyl racemic V-1631 Me Et Me NH Ph CH₂C(Me)₂ n-Undecyl (R)- V-1632 Me Me Me NH Ph CH₂C(Me)₂ Ph racemic V-1633 Me Me Me NH Ph CH₂C(Me)₂ Ph (R)- V-1634 Me Et Me NH Ph CH₂C(Me)₂ Ph racemic V-1635 Me Et Me NH Ph CH₂C(Me)₂ Ph (R)- V-1636 Me Me Me NH Ph CH₂C(Me)₂ OEt racemic V-1637 Me Me Me NH Ph CH₂C(Me)₂ OEt (R)- V-1638 Me Et Me NH Ph CH₂C(Me)₂ OEt racemic V-1639 Me Et Me NH Ph CH₂C(Me)₂ OEt (R)- V-1640 Me Me Me NH Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-1641 Me Me Me NH Ph CH₂C(Me)₂ (CH₂)₂COOH (R)- V-1642 Me Et Me NH Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-1643 Me Et Me NH Ph CH₂C(Me)₂ (CH₂)₂COOH (R)- V-1644 Me Me Me CH₂ Ph CH₂ Me racemic V-1645 Me Me Me CH₂ Ph CH₂ Me (S)- V-1646 Me Et Me CH₂ Ph CH₂ Me racemic V-1647 Me Et Me CH₂ Ph CH₂ Me (S)- V-1648 Me Me Me CH₂ Ph CH₂ Et racemic

TABLE 137 (Vc)

Compound No. R¹ R² R³ L² R⁴ L³ R⁶ Configuration V-1649 Me Me Me CH₂ Ph CH₂ Et (S)- V-1650 Me Et Me CH₂ Ph CH₂ Et racemic V-1651 Me Et Me CH₂ Ph CH₂ Et (S)- V-1652 Me Me Me CH₂ Ph CH₂ nPr racemic V-1653 Me Me Me CH₂ Ph CH₂ nPr (S)- V-1654 Me Et Me CH₂ Ph CH₂ nPr racemic V-1655 Me Et Me CH₂ Ph CH₂ nPr (S)- V-1656 Me Me Me CH₂ Ph CH₂ iPr racemic V-1657 Me Me Me CH₂ Ph CH₂ iPr (S)- V-1658 Me Et Me CH₂ Ph CH₂ iPr racemic V-1659 Me Et Me CH₂ Ph CH₂ iPr (S)- V-1660 Me Me Me CH₂ Ph CH₂ nBu racemic V-1661 Me Me Me CH₂ Ph CH₂ nBu (S)- V-1662 Me Et Me CH₂ Ph CH₂ nBu racemic V-1663 Me Et Me CH₂ Ph CH₂ nBu (S)- V-1664 Me Me Me CH₂ Ph CH₂ tBu racemic V-1665 Me Me Me CH₂ Ph CH₂ tBu (S)- V-1666 Me Et Me CH₂ Ph CH₂ tBu racemic V-1667 Me Et Me CH₂ Ph CH₂ tBu (S)- V-1668 Me Me Me CH₂ Ph CH₂ iBu racemic V-1669 Me Me Me CH₂ Ph CH₂ iBu (S)- V-1670 Me Et Me CH₂ Ph CH₂ iBu racemic V-1671 Me Et Me CH₂ Ph CH₂ iBu (S)- V-1672 Me Me Me CH₂ Ph CH₂ n-Heptyl racemic V-1673 Me Me Me CH₂ Ph CH₂ n-Heptyl (S)- V-1674 Me Et Me CH₂ Ph CH₂ n-Heptyl racemic V-1675 Me Et Me CH₂ Ph CH₂ n-Heptyl (S)- V-1676 Me Me Me CH₂ Ph CH₂ n-Undecyl racemic V-1677 Me Me Me CH₂ Ph CH₂ n-Undecyl (S)- V-1678 Me Et Me CH₂ Ph CH₂ n-Undecyl racemic V-1679 Me Et Me CH₂ Ph CH₂ n-Undecyl (S)- V-1680 Me Me Me CH₂ Ph CH₂ Ph racemic V-1681 Me Me Me CH₂ Ph CH₂ Ph (S)- V-1682 Me Et Me CH₂ Ph CH₂ Ph racemic V-1683 Me Et Me CH₂ Ph CH₂ Ph (S)- V-1684 Me Me Me CH₂ Ph CH₂ OEt racemic V-1685 Me Me Me CH₂ Ph CH₂ OEt (S)- V-1686 Me Et Me CH₂ Ph CH₂ OEt racemic V-1687 Me Et Me CH₂ Ph CH₂ OEt (S)- V-1688 Me Me Me CH₂ Ph CH₂ (CH₂)₂COOH racemic V-1689 Me Me Me CH₂ Ph CH₂ (CH₂)₂COOH (S)- V-1690 Me Et Me CH₂ Ph CH₂ (CH₂)₂COOH racemic V-1691 Me Et Me CH₂ Ph CH₂ (CH₂)₂COOH (S)- V-1692 Me Me Me CH₂ Ph — Me racemic V-1693 Me Me Me CH₂ Ph — Me (S)- V-1694 Me Et Me CH₂ Ph — Me racemic V-1695 Me Et Me CH₂ Ph — Me (S)- V-1696 Me Me Me CH₂ Ph — Et racemic V-1697 Me Me Me CH₂ Ph — Et (S)- V-1698 Me Et Me CH₂ Ph — Et racemic

TABLE 138 (Vc)

Com- pound No. R¹ R² R³ L² R⁴ L³ R⁶ Configuration V-1699 Me Et Me CH₂ Ph — Et (S)- V-1700 Me Me Me CH₂ Ph — nPr racemic V-1701 Me Me Me CH₂ Ph — nPr (S)- V-1702 Me Et Me CH₂ Ph — nPr racemic V-1703 Me Et Me CH₂ Ph — nPr (S)- V-1704 Me Me Me CH₂ Ph — iPr racemic V-1705 Me Me Me CH₂ Ph — iPr (S)- V-1706 Me Et Me CH₂ Ph — iPr racemic V-1707 Me Et Me CH₂ Ph — iPr (S)- V-1708 Me Me Me CH₂ Ph — nBu racemic V-1709 Me Me Me CH₂ Ph — nBu (S)- V-1710 Me Et Me CH₂ Ph — nBu racemic V-1711 Me Et Me CH₂ Ph — nBu (S)- V-1712 Me Me Me CH₂ Ph — tBu racemic V-1713 Me Me Me CH₂ Ph — tBu (S)- V-1714 Me Et Me CH₂ Ph — tBu racemic V-1715 Me Et Me CH₂ Ph — tBu (S)- V-1716 Me Me Me CH₂ Ph — iBu racemic V-1717 Me Me Me CH₂ Ph — iBu (S)- V-1718 Me Et Me CH₂ Ph — iBu racemic V-1719 Me Et Me CH₂ Ph — iBu (S)- V-1720 Me Me Me CH₂ Ph — n-Heptyl racemic V-1721 Me Me Me CH₂ Ph — n-Heptyl (S)- V-1722 Me Et Me CH₂ Ph — n-Heptyl racemic V-1723 Me Et Me CH₂ Ph — n-Heptyl (S)- V-1724 Me Me Me CH₂ Ph — n-Undecyl racemic V-1725 Me Me Me CH₂ Ph — n-Undecyl (S)- V-1726 Me Et Me CH₂ Ph — n-Undecyl racemic V-1727 Me Et Me CH₂ Ph — n-Undecyl (S)- V-1728 Me Me Me CH₂ Ph — Ph racemic V-1729 Me Me Me CH₂ Ph — Ph (S)- V-1730 Me Et Me CH₂ Ph — Ph racemic V-1731 Me Et Me CH₂ Ph — Ph (S)- V-1732 Me Me Me CH₂ Ph — OEt racemic V-1733 Me Me Me CH₂ Ph — OEt (S)- V-1734 Me Et Me CH₂ Ph — OEt racemic V-1735 Me Et Me CH₂ Ph — OEt (S)- V-1736 Me Me Me CH₂ Ph — (CH₂)₂COOH racemic V-1737 Me Me Me CH₂ Ph — (CH₂)₂COOH (S)- V-1738 Me Et Me CH₂ Ph — (CH₂)₂COOH racemic V-1739 Me Et Me CH₂ Ph — (CH₂)₂COOH (S)- V-1740 Me Me Me CH₂ Ph C(Me)₂ Me racemic V-1741 Me Me Me CH₂ Ph C(Me)₂ Me (S)- V-1742 Me Et Me CH₂ Ph C(Me)₂ Me racemic V-1743 Me Et Me CH₂ Ph C(Me)₂ Me (S)- V-1744 Me Me Me CH₂ Ph C(Me)₂ Et racemic V-1745 Me Me Me CH₂ Ph C(Me)₂ Et (S)- V-1746 Me Et Me CH₂ Ph C(Me)₂ Et racemic V-1747 Me Et Me CH₂ Ph C(Me)₂ Et (S)- V-1748 Me Me Me CH₂ Ph C(Me)₂ nPr racemic

TABLE 139 (Vc)

Com- pound No. R¹ R² R³ L² R⁴ L³ R⁶ Configuration V-1749 Me Me Me CH₂ Ph C(Me)₂ nPr (S)- V-1750 Me Et Me CH₂ Ph C(Me)₂ nPr racemic V-1751 Me Et Me CH₂ Ph C(Me)₂ nPr (S)- V-1752 Me Me Me CH₂ Ph C(Me)₂ iPr racemic V-1753 Me Me Me CH₂ Ph C(Me)₂ iPr (S)- V-1754 Me Et Me CH₂ Ph C(Me)₂ iPr racemic V-1755 Me Et Me CH₂ Ph C(Me)₂ iPr (S)- V-1756 Me Me Me CH₂ Ph C(Me)₂ nBu racemic V-1757 Me Me Me CH₂ Ph C(Me)₂ nBu (S)- V-1758 Me Et Me CH₂ Ph C(Me)₂ nBu racemic V-1759 Me Et Me CH₂ Ph C(Me)₂ nBu (S)- V-1760 Me Me Me CH₂ Ph C(Me)₂ tBu racemic V-1761 Me Me Me CH₂ Ph C(Me)₂ tBu (S)- V-1762 Me Et Me CH₂ Ph C(Me)₂ tBu racemic V-1763 Me Et Me CH₂ Ph C(Me)₂ tBu (S)- V-1764 Me Me Me CH₂ Ph C(Me)₂ iBu racemic V-1765 Me Me Me CH₂ Ph C(Me)₂ iBu (S)- V-1766 Me Et Me CH₂ Ph C(Me)₂ iBu racemic V-1767 Me Et Me CH₂ Ph C(Me)₂ iBu (S)- V-1768 Me Me Me CH₂ Ph C(Me)₂ n-Heptyl racemic V-1769 Me Me Me CH₂ Ph C(Me)₂ n-Heptyl (S)- V-1770 Me Et Me CH₂ Ph C(Me)₂ n-Heptyl racemic V-1771 Me Et Me CH₂ Ph C(Me)₂ n-Heptyl (S)- V-1772 Me Me Me CH₂ Ph C(Me)₂ n-Undecyl racemic V-1773 Me Me Me CH₂ Ph C(Me)₂ n-Undecyl (S)- V-1774 Me Et Me CH₂ Ph C(Me)₂ n-Undecyl racemic V-1775 Me Et Me CH₂ Ph C(Me)₂ n-Undecyl (S)- V-1776 Me Me Me CH₂ Ph C(Me)₂ Ph racemic V-1777 Me Me Me CH₂ Ph C(Me)₂ Ph (S)- V-1778 Me Et Me CH₂ Ph C(Me)₂ Ph racemic V-1779 Me Et Me CH₂ Ph C(Me)₂ Ph (S)- V-1780 Me Me Me CH₂ Ph C(Me)₂ OEt racemic V-1781 Me Me Me CH₂ Ph C(Me)₂ OEt (S)- V-1782 Me Et Me CH₂ Ph C(Me)₂ OEt racemic V-1783 Me Et Me CH₂ Ph C(Me)₂ OEt (S)- V-1784 Me Me Me CH₂ Ph C(Me)₂ (CH₂)₂COOH racemic V-1785 Me Me Me CH₂ Ph C(Me)₂ (CH₂)₂COOH (S)- V-1786 Me Et Me CH₂ Ph C(Me)₂ (CH₂)₂COOH racemic V-1787 Me Et Me CH₂ Ph C(Me)₂ (CH₂)₂COOH (S)- V-1788 Me Me Me CH₂ Ph (CH₂)₂ Me racemic V-1789 Me Me Me CH₂ Ph (CH₂)₂ Me (S)- V-1790 Me Et Me CH₂ Ph (CH₂)₂ Me racemic V-1791 Me Et Me CH₂ Ph (CH₂)₂ Me (S)- V-1792 Me Me Me CH₂ Ph (CH₂)₂ Et racemic V-1793 Me Me Me CH₂ Ph (CH₂)₂ Et (S)- V-1794 Me Et Me CH₂ Ph (CH₂)₂ Et racemic V-1795 Me Et Me CH₂ Ph (CH₂)₂ Et (S)- V-1796 Me Me Me CH₂ Ph (CH₂)₂ nPr racemic V-1797 Me Me Me CH₂ Ph (CH₂)₂ nPr (S)- V-1798 Me Et Me CH₂ Ph (CH₂)₂ nPr racemic

TABLE 140 (Vc)

Com- Con- pound figu- No. R¹ R² R³ L² R⁴ L³ R⁶ ration V-1799 Me Et Me CH₂ Ph (CH₂)₂ nPr (S)- V-1800 Me Me Me CH₂ Ph (CH₂)₂ iPr racemic V-1801 Me Me Me CH₂ Ph (CH₂)₂ iPr (S)- V-1802 Me Et Me CH₂ Ph (CH₂)₂ iPr racemic V-1803 Me Et Me CH₂ Ph (CH₂)₂ iPr (S)- V-1804 Me Me Me CH₂ Ph (CH₂)₂ nBu racemic V-1805 Me Me Me CH₂ Ph (CH₂)₂ nBu (S)- V-1806 Me Et Me CH₂ Ph (CH₂)₂ nBu racemic V-1807 Me Et Me CH₂ Ph (CH₂)₂ nBu (S)- V-1808 Me Me Me CH₂ Ph (CH₂)₂ tBu racemic V-1809 Me Me Me CH₂ Ph (CH₂)₂ tBu (S)- V-1810 Me Et Me CH₂ Ph (CH₂)₂ tBu racemic V-1811 Me Et Me CH₂ Ph (CH₂)₂ tBu (S)- V-1812 Me Me Me CH₂ Ph (CH₂)₂ iBu racemic V-1813 Me Me Me CH₂ Ph (CH₂)₂ iBu (S)- V-1814 Me Et Me CH₂ Ph (CH₂)₂ iBu racemic V-1815 Me Et Me CH₂ Ph (CH₂)₂ iBu (S)- V-1816 Me Me Me CH₂ Ph (CH₂)₂ n-Heptyl racemic V-1817 Me Me Me CH₂ Ph (CH₂)₂ n-Heptyl (S)- V-1818 Me Et Me CH₂ Ph (CH₂)₂ n-Heptyl racemic V-1819 Me Et Me CH₂ Ph (CH₂)₂ n-Heptyl (S)- V-1820 Me Me Me CH₂ Ph (CH₂)₂ n-Undecyl racemic V-1821 Me Me Me CH₂ Ph (CH₂)₂ n-Undecyl (S)- V-1822 Me Et Me CH₂ Ph (CH₂)₂ n-Undecyl racemic V-1823 Me Et Me CH₂ Ph (CH₂)₂ n-Undecyl (S)- V-1824 Me Me Me CH₂ Ph (CH₂)₂ Ph racemic V-1825 Me Me Me CH₂ Ph (CH₂)₂ Ph (S)- V-1826 Me Et Me CH₂ Ph (CH₂)₂ Ph racemic V-1827 Me Et Me CH₂ Ph (CH₂)₂ Ph (S)- V-1828 Me Me Me CH₂ Ph (CH₂)₂ OEt racemic V-1829 Me Me Me CH₂ Ph (CH₂)₂ OEt (S)- V-1830 Me Et Me CH₂ Ph (CH₂)₂ OEt racemic V-1831 Me Et Me CH₂ Ph (CH₂)₂ OEt (S)- V-1832 Me Me Me CH₂ Ph (CH₂)₂ (CH₂)₂COOH racemic V-1833 Me Me Me CH₂ Ph (CH₂)₂ (CH₂)₂COOH (S)- V-1834 Me Et Me CH₂ Ph (CH₂)₂ (CH₂)₂COOH racemic V-1835 Me Et Me CH₂ Ph (CH₂)₂ (CH₂)₂COOH (S)- V-1836 Me Me Me CH₂ Ph CH₂C(Me)₂ Me racemic V-1837 Me Me Me CH₂ Ph CH₂C(Me)₂ Me (S)- V-1838 Me Et Me CH₂ Ph CH₂C(Me)₂ Me racemic V-1839 Me Et Me CH₂ Ph CH₂C(Me)₂ Me (S)- V-1840 Me Me Me CH₂ Ph CH₂C(Me)₂ Et racemic V-1841 Me Me Me CH₂ Ph CH₂C(Me)₂ Et (S)- V-1842 Me Et Me CH₂ Ph CH₂C(Me)₂ Et racemic V-1843 Me Et Me CH₂ Ph CH₂C(Me)₂ Et (S)- V-1844 Me Me Me CH₂ Ph CH₂C(Me)₂ nPr racemic V-1845 Me Me Me CH₂ Ph CH₂C(Me)₂ nPr (S)- V-1846 Me Et Me CH₂ Ph CH₂C(Me)₂ nPr racemic V-1847 Me Et Me CH₂ Ph CH₂C(Me)₂ nPr (S)- V-1848 Me Me Me CH₂ Ph CH₂C(Me)₂ iPr racemic

TABLE 141 (Vc)

Com- Con- pound figu- No. R¹ R² R³ L² R⁴ L³ R⁶ ration V-1849 Me Me Me CH₂ Ph CH₂C(Me)₂ iPr (S)- V-1850 Me Et Me CH₂ Ph CH₂C(Me)₂ iPr racemic V-1851 Me Et Me CH₂ Ph CH₂C(Me)₂ iPr (S)- V-1852 Me Me Me CH₂ Ph CH₂C(Me)₂ nBu racemic V-1853 Me Me Me CH₂ Ph CH₂C(Me)₂ nBu (S)- V-1854 Me Et Me CH₂ Ph CH₂C(Me)₂ nBu racemic V-1855 Me Et Me CH₂ Ph CH₂C(Me)₂ nBu (S)- V-1856 Me Me Me CH₂ Ph CH₂C(Me)₂ tBu racemic V-1857 Me Me Me CH₂ Ph CH₂C(Me)₂ tBu (S)- V-1858 Me Et Me CH₂ Ph CH₂C(Me)₂ tBu racemic V-1859 Me Et Me CH₂ Ph CH₂C(Me)₂ tBu (S)- V-1860 Me Me Me CH₂ Ph CH₂C(Me)₂ iBu racemic V-1861 Me Me Me CH₂ Ph CH₂C(Me)₂ iBu (S)- V-1862 Me Et Me CH₂ Ph CH₂C(Me)₂ iBu racemic V-1863 Me Et Me CH₂ Ph CH₂C(Me)₂ iBu (S)- V-1864 Me Me Me CH₂ Ph CH₂C(Me)₂ n-Heptyl racemic V-1865 Me Me Me CH₂ Ph CH₂C(Me)₂ n-Heptyl (S)- V-1866 Me Et Me CH₂ Ph CH₂C(Me)₂ n-Heptyl racemic V-1867 Me Et Me CH₂ Ph CH₂C(Me)₂ n-Heptyl (S)- V-1868 Me Me Me CH₂ Ph CH₂C(Me)₂ n-Undecyl racemic V-1869 Me Me Me CH₂ Ph CH₂C(Me)₂ n-Undecyl (S)- V-1870 Me Et Me CH₂ Ph CH₂C(Me)₂ n-Undecyl racemic V-1871 Me Et Me CH₂ Ph CH₂C(Me)₂ n-Undecyl (S)- V-1872 Me Me Me CH₂ Ph CH₂C(Me)₂ Ph racemic V-1873 Me Me Me CH₂ Ph CH₂C(Me)₂ Ph (S)- V-1874 Me Et Me CH₂ Ph CH₂C(Me)₂ Ph racemic V-1875 Me Et Me CH₂ Ph CH₂C(Me)₂ Ph (S)- V-1876 Me Me Me CH₂ Ph CH₂C(Me)₂ OEt racemic V-1877 Me Me Me CH₂ Ph CH₂C(Me)₂ OEt (S)- V-1878 Me Et Me CH₂ Ph CH₂C(Me)₂ OEt racemic V-1879 Me Et Me CH₂ Ph CH₂C(Me)₂ OEt (S)- V-1880 Me Me Me CH₂ Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-1881 Me Me Me CH₂ Ph CH₂C(Me)₂ (CH₂)₂COOH (S)- V-1882 Me Et Me CH₂ Ph CH₂C(Me)₂ (CH₂)₂COOH racemic V-1883 Me Et Me CH₂ Ph CH₂C(Me)₂ (CH₂)₂COOH (S)-

TABLE 142 (Vc)

Com- pound No. R¹ R² R³ L² R⁴ L³ R⁶ Configuration V-2060 Me Me Me — Ph — Me racemic V-2061 Me Me Me — Ph — Me (R)- V-2062 Me Et Me — Ph — Me racemic V-2063 Me Et Me — Ph — Me (R)- V-2064 Me Me Me — Ph — Et racemic V-2065 Me Me Me — Ph — Et (R)- V-2066 Me Et Me — Ph — Et racemic V-2067 Me Et Me — Ph — Et (R)- V-2068 Me Me Me — Ph — nPr racemic V-2069 Me Me Me — Ph — nPr (R)- V-2070 Me Et Me — Ph — nPr racemic V-2071 Me Et Me — Ph — nPr (R)- V-2072 Me Me Me — Ph — iPr racemic V-2073 Me Me Me — Ph — iPr (R)- V-2074 Me Et Me — Ph — iPr racemic V-2075 Me Et Me — Ph — iPr (R)- V-2076 Me Me Me — Ph — nBu racemic V-2077 Me Me Me — Ph — nBu (R)- V-2078 Me Et Me — Ph — nBu racemic V-2079 Me Et Me — Ph — nBu (R)- V-2080 Me Me Me — Ph — tBu racemic V-2081 Me Me Me — Ph — tBu (R)- V-2082 Me Et Me — Ph — tBu racemic V-2083 Me Et Me — Ph — tBu (R)- V-2084 Me Me Me — Ph — iBu racemic V-2085 Me Me Me — Ph — iBu (R)- V-2086 Me Et Me — Ph — iBu racemic V-2087 Me Et Me — Ph — iBu (R)- V-2088 Me Me Me — Ph — n-Heptyl racemic V-2089 Me Me Me — Ph — n-Heptyl (R)- V-2090 Me Et Me — Ph — n-Heptyl racemic V-2091 Me Et Me — Ph — n-Heptyl (R)- V-2092 Me Me Me — Ph — n-Undecyl racemic V-2093 Me Me Me — Ph — n-Undecyl (R)- V-2094 Me Et Me — Ph — n-Undecyl racemic V-2095 Me Et Me — Ph — n-Undecyl (R)- V-2096 Me Me Me — Ph — OEt racemic V-2097 Me Me Me — Ph — OEt (R)- V-2098 Me Et Me — Ph — OEt racemic V-2099 Me Et Me — Ph — OEt (R)- V-2100 Me Me Me — Ph — (CH₂)₂COONa racemic V-2101 Me Me Me — Ph — (CH₂)₂COONa (R)- V-2102 Me Et Me — Ph — (CH₂)₂COONa racemic V-2103 Me Et Me — Ph — (CH₂)₂COONa (R)- V-2104 Me Me Me — Ph CH₂ Me racemic V-2105 Me Me Me — Ph CH₂ Me (S)- V-2106 Me Et Me — Ph CH₂ Me racemic V-2107 Me Et Me — Ph CH₂ Me (S)- V-2108 Me Me Me — Ph CH₂ Et racemic V-2109 Me Me Me — Ph CH₂ Et (S)-

TABLE 143 (Vc)

Com- pound No. R¹ R² R³ L² R⁴ L³ R⁶ Configuration V-2110 Me Et Me — Ph CH₂ Et racemic V-2111 Me Et Me — Ph CH₂ Et (S)- V-2112 Me Me Me — Ph CH₂ nPr racemic V-2113 Me Me Me — Ph CH₂ nPr (S)- V-2114 Me Et Me — Ph CH₂ nPr racemic V-2115 Me Et Me — Ph CH₂ nPr (S)- V-2116 Me Me Me — Ph CH₂ iPr racemic V-2117 Me Me Me — Ph CH₂ iPr (S)- V-2118 Me Et Me — Ph CH₂ iPr racemic V-2119 Me Et Me — Ph CH₂ iPr (S)- V-2120 Me Me Me — Ph CH₂ nBu racemic V-2121 Me Me Me — Ph CH₂ nBu (S)- V-2122 Me Et Me — Ph CH₂ nBu racemic V-2123 Me Et Me — Ph CH₂ nBu (S)- V-2124 Me Me Me — Ph CH₂ tBu racemic V-2125 Me Me Me — Ph CH₂ tBu (S)- V-2126 Me Et Me — Ph CH₂ tBu racemic V-2127 Me Et Me — Ph CH₂ tBu (S)- V-2128 Me Me Me — Ph CH₂ iBu racemic V-2129 Me Me Me — Ph CH₂ iBu (S)- V-2130 Me Et Me — Ph CH₂ iBu racemic V-2131 Me Et Me — Ph CH₂ iBu (S)- V-2132 Me Me Me — Ph CH₂ n-Heptyl racemic V-2133 Me Me Me — Ph CH₂ n-Heptyl (S)- V-2134 Me Et Me — Ph CH₂ n-Heptyl racemic V-2135 Me Et Me — Ph CH₂ n-Heptyl (S)- V-2136 Me Me Me — Ph CH₂ n-Undecyl racemic V-2137 Me Me Me — Ph CH₂ n-Undecyl (S)- V-2138 Me Et Me — Ph CH₂ n-Undecyl racemic V-2139 Me Et Me — Ph CH₂ n-Undecyl (S)- V-2140 Me Me Me — Ph CH₂ OEt racemic V-2141 Me Me Me — Ph CH₂ OEt (S)- V-2142 Me Et Me — Ph CH₂ OEt racemic V-2143 Me Et Me — Ph CH₂ OEt (S)- V-2144 Me Me Me — Ph CH₂ (CH₂)₂COONa racemic V-2145 Me Me Me — Ph CH₂ (CH₂)₂COONa (S)- V-2146 Me Et Me — Ph CH₂ (CH₂)₂COONa racemic V-2147 Me Et Me — Ph CH₂ (CH₂)₂COONa (S)-

TABLE 144 (VIa)

Compound No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ Configuration VI-1  Me Me Me O Ph CH₂ H H Me racemic VI-2  Me Me Me O Ph CH₂ H H Me (S)- VI-3  Me Me Me O Ph CH₂ Me H Me racemic VI-4  Me Me Me O Ph CH₂ Me H Me (S)- VI-5  Me Me Me O Ph CH₂ H Me Me racemic VI-6  Me Me Me O Ph CH₂ H Me Me (S)- VI-7  Me Me Me O Ph CH₂ Me Me Me racemic VI-8  Me Me Me O Ph CH₂ Me Me Me (S)- VI-9  Me Et Me O Ph CH₂ H H Me racemic VI-10 Me Et Me O Ph CH₂ H H Me (S)- VI-11 Me Et Me O Ph CH₂ Me H Me racemic VI-12 Me Et Me O Ph CH₂ Me H Me (S)- VT-13 Me Et Me O Ph CH₂ H Me Me racemic VI-14 Me Et Me O Ph CH₂ H Me Me (S)- VI-15 Me Et Me O Ph CH₂ Me Me Me racemic VI-16 Me Et Me O Ph CH₂ Me Me Me (S)- VI-17 Me Me Me O Ph CH₂ H H Et racemic VI-18 Me Me Me O Ph CH₂ H H Et (S)- VI-19 Me Me Me O Ph CH₂ Me H Et racemic VI-20 Me Me Me O Ph CH₂ Me H Et (S)- VI-21 Me Me Me O Ph CH₂ H Me Et racemic VI-22 Me Me Me O Ph CH₂ H Me Et (S)- VI-23 Me Me Me O Ph CH₂ Me Me Et racemic VI-24 Me Me Me O Ph CH₂ Me Me Et (S)- VI-25 Me Et Me O Ph CH₂ H H Et racemic VI-26 Me Et Me O Ph CH₂ H H Et (S)- VI-27 Me Et Me O Ph CH₂ Me H Et racemic VI-28 Me Et Me O Ph CH₂ Me H Et (S)- VI-29 Me Et Me O Ph CH₂ H Me Et racemic VI-30 Me Et Me O Ph CH₂ H Me Et (S)- VI-31 Me Et Me O Ph CH₂ Me Me Et racemic VI-32 Me Et Me O Ph CH₂ Me Me Et (S)- VI-33 Me Me Me NH Ph CH₂ H H Me racemic VI-34 Me Me Me NH Ph CH₂ H H Me (S)- VI-35 Me Me Me NH Ph CH₂ Me H Me racemic VI-36 Me Me Me NH Ph CH₂ Me H Me (S)- VI-37 Me Me Me NH Ph CH₂ H Me Me racemic VI-38 Me Me Me NH Ph CH₂ H Me Me (S)- VI-39 Me Me Me NH Ph CH₂ Me Me Me racemic VI-40 Me Me Me NH Ph CH₂ Me Me Me (S)- VI-41 Me Et Me NH Ph CH₂ H H Me racemic VI-42 Me Et Me NH Ph CH₂ H H Me (S)- VI-43 Me Et Me NH Ph CH₂ Me H Me racemic VI-44 Me Et Me NH Ph CH₂ Me H Me (S)- VI-45 Me Et Me NH Ph CH₂ H Me Me racemic VI-46 Me Et Me NH Ph CH₂ H Me Me (S)- VI-47 Me Et Me NH Ph CH₂ Me Me Me racemic VI-48 Me Et Me NH Ph CH₂ Me Me Me (S)- VI-49 Me Me Me NH Ph CH₂ H H Et racemic VI-50 Me Me Me NH Ph CH₂ H H Et (S)-

TABLE 145 (VIa)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ uration VI-51 Me Me Me NH Ph CH₂ Me H Et racemic VI-52 Me Me Me NH Ph CH₂ Me H Et (S)- VI-53 Me Me Me NH Ph CH₂ H Me Et racemic VI-54 Me Me Me NH Ph CH₂ H Me Et (S)- VI-55 Me Me Me NH Ph CH₂ Me Me Et racemic VI-56 Me Me Me NH Ph CH₂ Me Me Et (S)- VI-57 Me Et Me NH Ph CH₂ H H Et racemic VI-58 Me Et Me NH Ph CH₂ H H Et (S)- VI-59 Me Et Me NH Ph CH₂ Me H Et racemic VI-60 Me Et Me NH Ph CH₂ Me H Et (S)- VI-61 Me Et Me NH Ph CH₂ H Me Et racemic VI-62 Me Et Me NH Ph CH₂ H Me Et (S)- VI-63 Me Et Me NH Ph CH₂ Me Me Et racemic VI-64 Me Et Me NH Ph CH₂ Me Me Et (S)- VI-65 Me Me Me NH Ph CH₂ H H C(═O)Me racemic VI-66 Me Me Me NH Ph CH₂ H H C(═O)Me (S)- VI-67 Me Me Me NH Ph CH₂ Me H C(═O)Me racemic VI-68 Me Me Me NH Ph CH₂ Me H C(═O)Me (S)- VI-69 Me Me Me NH Ph CH₂ H Me C(═O)Me racemic VI-70 Me Me Me NH Ph CH₂ H Me C(═O)Me (S)- VI-71 Me Me Me NH Ph CH₂ Me Me C(═O)Me racemic VI-72 Me Me Me NH Ph CH₂ Me Me C(═O)Me (S)- VI-73 Me Et Me NH Ph CH₂ H H C(═O)Me racemic VI-74 Me Et Me NH Ph CH₂ H H C(═O)Me (S)- VI-75 Me Et Me NH Ph CH₂ Me H C(═O)Me racemic VI-76 Me Et Me NH Ph CH₂ Me H C(═O)Me (S)- VI-77 Me Et Me NH Ph CH₂ H Me C(═O)Me racemic VI-78 Me Et Me NH Ph CH₂ H Me C(═O)Me (S)- VI-79 Me Et Me NH Ph CH₂ Me Me C(═O)Me racemic VI-80 Me Et Me NH Ph CH₂ Me Me C(═O)Me (S)- VI-81 Me Me Me NH Ph CH₂ H H C(═O)Et racemic VI-82 Me Me Me NH Ph CH₂ H H C(═O)Et (S)- VI-83 Me Me Me NH Ph CH₂ Me H C(═O)Et racemic VI-84 Me Me Me NH Ph CH₂ Me H C(═O)Et (S)- VI-85 Me Me Me NH Ph CH₂ H Me C(═O)Et racemic VI-86 Me Me Me NH Ph CH₂ H Me C(═O)Et (S)- VI-87 Me Me Me NH Ph CH₂ Me Me C(═O)Et racemic VI-88 Me Me Me NH Ph CH₂ Me Me C(═O)Et (S)- VI-89 Me Et Me NH Ph CH₂ H H C(═O)Et racemic VI-90 Me Et Me NH Ph CH₂ H H C(═O)Et (S)- VI-91 Me Et Me NH Ph CH₂ Me H C(═O)Et racemic VI-92 Me Et Me NH Ph CH₂ Me H C(═O)Et (S)- VI-93 Me Et Me NH Ph CH₂ H Me C(═O)Et racemic VI-94 Me Et Me NH Ph CH₂ H Me C(═O)Et (S)- VI-95 Me Et Me NH Ph CH₂ Me Me C(═O)Et racemic VI-96 Me Et Me NH Ph CH₂ Me Me C(═O)Et (S)- VI-97 Me Me Me NH Ph CH₂ H H C(═O)tBu racemic VI-98 Me Me Me NH Ph CH₂ H H C(═O)tBu (S)- VI-99 Me Me Me NH Ph CH₂ Me H C(═O)tBu racemic VI-100 Me Me Me NH Ph CH₂ Me H C(═O)tBu (S)-

TABLE 146 (VIa)

Compound No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ Configuration VI-101 Me Me Me NH Ph CH₂ H Me C(═O)tBu racemic VI-102 Me Me Me NH Ph CH₂ H Me C(═O)tBu (S)- VI-103 Me Me Me NH Ph CH₂ Me Me C(═O)tBu racemic VI-104 Me Me Me NH Ph CH₂ Me Me C(═O)tBu (S)- VI-105 Me Et Me NH Ph CH₂ H H C(═O)tBu racemic VI-106 Me Et Me NH Ph CH₂ H H C(═O)tBu (S)- VI-107 Me Et Me NH Ph CH₂ Me H C(═O)tBu racemic VI-108 Me Et Me NH Ph CH₂ Me H C(═O)tBu (S)- VI-109 Me Et Me NH Ph CH₂ H Me C(═O)tBu racemic VI-110 Me Et Me NH Ph CH₂ H Me C(═O)tBu (S)- VI-111 Me Et Me NH Ph CH₂ Me Me C(═O)tBu racemic VI-112 Me Et Me NH Ph CH₂ Me Me C(═O)tBu (S)- VI-113 Me Me Me NH Ph CH₂ H H C(═O)OEt racemic VI-114 Me Me Me NH Ph CH₂ H H C(═O)OEt (S)- VI-115 Me Me Me NH Ph CH₂ Me H C(═O)OEt racemic VI-116 Me Me Me NH Ph CH₂ Me H C(═O)OEt (S)- VI-117 Me Me Me NH Ph CH₂ H Me C(═O)OEt racemic VI-118 Me Me Me NH Ph CH₂ H Me C(═O)OEt (S)- VI-119 Me Me Me NH Ph CH₂ Me Me C(═O)OEt racemic VI-120 Me Me Me NH Ph CH₂ Me Me C(═O)OEt (S)- VI-121 Me Et Me NH Ph CH₂ H H C(═O)OEt racemic VI-122 Me Et Me NH Ph CH₂ H H C(═O)OEt (S)- VI-123 Me Et Me NH Ph CH₂ Me H C(═O)OEt racemic VI-124 Me Et Me NH Ph CH₂ Me H C(═O)OEt (S)- VI-125 Me Et Me NH Ph CH₂ H Me C(═O)OEt racemic VI-126 Me Et Me NH Ph CH₂ H Me C(═O)OEt (S)- VI-127 Me Et Me NH Ph CH₂ Me Me C(═O)OEt racemic VI-128 Me Et Me NH Ph CH₂ Me Me C(═O)OEt (S)- VI-129 Me Me Me NH Ph CH₂ H H C(═O)OcHex racemic VI-130 Me Me Me NH Ph CH₂ H H C(═O)OcHex (S)- VI-131 Me Me Me NH Ph CH₂ Me H C(═O)OcHex racemic VI-132 Me Me Me NH Ph CH₂ Me H C(═O)OcHex (S)- VI-133 Me Me Me NH Ph CH₂ H Me C(═O)OcHex cracemic VI-134 Me Me Me NH Ph CH₂ H Me C(═O)OcHex (S)- VI-135 Me Me Me NH Ph CH₂ Me Me C(═O)OcHex racemic VI-136 Me Me Me NH Ph CH₂ Me Me C(═O)OcHex (S)- VI-137 Me Et Me NH Ph CH₂ H H C(═O)OcHex racemic VI-138 Me Et Me NH Ph CH₂ H H C(═O)OcHex (S)- VI-139 Me Et Me NH Ph CH₂ Me H C(═O)OcHex racemic VI-140 Me Et Me NH Ph CH₂ Me H C(═O)OcHex (S)- VI-141 Me Et Me NH Ph CH₂ H Me C(═O)OcHex racemic VI-142 Me Et Me NH Ph CH₂ H Me C(═O)OcHex (S)- VI-143 Me Et Me NH Ph CH₂ Me Me C(═O)OcHex racemic VI-144 Me Et Me NH Ph CH₂ Me Me C(═O)OcHex (S)- VI-145 Me Me Me CH₂ Ph CH₂ H H Me racemic VI-146 Me Me Me CH₂ Ph CH₂ H H Me (S)- VI-147 Me Me Me CH₂ Ph CH₂ Me H Me racemic VI-148 Me Me Me CH₂ Ph CH₂ Me H Me (S)- VI-149 Me Me Me CH₂ Ph CH₂ H Me Me racemic VI-150 Me Me Me CH₂ Ph CH₂ H Me Me (S)-

TABLE 147 (VIa)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ uration VI-151 Me Me Me CH2 Ph CH₂ Me Me Me racemic VI-152 Me Me Me CH2 Ph CH₂ Me Me Me (S)- VI-153 Me Et Me CH2 Ph CH₂ H H Me racemic VI-154 Me Et Me CH2 Ph CH₂ H H Me (S)- VI-155 Me Et Me CH2 Ph CH₂ Me H Me racemic VI-156 Me Et Me CH2 Ph CH₂ Me H Me (S)- VI-157 Me Et Me CH2 Ph CH₂ H Me Me racemic VI-158 Me Et Me CH2 Ph CH₂ H Me Me (S)- VI-159 Me Et Me CH2 Ph CH₂ Me Me Me racemic VI-160 Me Et Me CH2 Ph CH₂ Me Me Me (S)- VI-161 Me Me Me CH2 Ph CH₂ H H Et racemic VI-162 Me Me Me CH2 Ph CH₂ H H Et (S)- VI-163 Me Me Me CH2 Ph CH₂ Me H Et racemic VI-164 Me Me Me CH2 Ph CH₂ Me H Et (S)- VI-165 Me Me Me CH2 Ph CH₂ H Me Et racemic VI-166 Me Me Me CH2 Ph CH₂ H Me Et (S)- VI-167 Me Me Me CH2 Ph CH₂ Me Me Et racemic VI-168 Me Me Me CH2 Ph CH₂ Me Me Et (S)- VI-169 Me Et Me CH2 Ph CH₂ H H Et racemic VI-170 Me Et Me CH2 Ph CH₂ H H Et (S)- VI-171 Me Et Me CH2 Ph CH₂ Me H Et racemic VI-172 Me Et Me CH2 Ph CH₂ Me H Et (S)- VI-173 Me Et Me CH2 Ph CH₂ H Me Et racemic VI-174 Me Et Me CH2 Ph CH₂ H Me Et (S)- VI-175 Me Et Me CH2 Ph CH₂ Me Me Et racemic VI-176 Me Et Me CH2 Ph CH₂ Me Me Et (S)-

TABLE 148 (VIa)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ uration VI-553 Me Me Me NH Ph (CH₂)₂ H H Me racemic VI-554 Me Me Me NH Ph (CH₂)₂ H H Me (R)- VI-555 Me Me Me NH Ph (CH₂)₂ Me H Me racemic VI-556 Me Me Me NH Ph (CH₂)₂ Me H Me (R)- VI-557 Me Me Me NH Ph (CH₂)₂ H Me Me racemic VI-558 Me Me Me NH Ph (CH₂)₂ H Me Me (R)- VI-559 Me Me Me NH Ph (CH₂)₂ Me Me Me racemic VI-560 Me Me Me NH Ph (CH₂)₂ Me Me Me (R)- VI-561 Me Et Me NH Ph (CH₂)₂ H H Me racemic VI-562 Me Et Me NH Ph (CH₂)₂ H H Me (R)- VI-563 Me Et Me NH Ph (CH₂)₂ Me H Me racemic VI-564 Me Et Me NH Ph (CH₂)₂ Me H Me (R)- VI-565 Me Et Me NH Ph (CH₂)₂ H Me Me racemic VI-566 Me Et Me NH Ph (CH₂)₂ H Me Me (R)- VI-567 Me Et Me NH Ph (CH₂)₂ Me Me Me racemic VI-568 Me Et Me NH Ph (CH₂)₂ Me Me Me (R)- VI-569 Me Me Me NH Ph (CH₂)₂ H H C(═O)Me racemic VI-570 Me Me Me NH Ph (CH₂)₂ H H C(═O)Me (R)- VI-571 Me Me Me NH Ph (CH₂)₂ Me H C(═O)Me racemic VI-572 Me Me Me NH Ph (CH₂)₂ Me H C(═O)Me (R)- VI-573 Me Me Me NH Ph (CH₂)₂ H Me C(═O)Me racemic VI-574 Me Me Me NH Ph (CH₂)₂ H Me C(═O)Me (R)- VI-575 Me Me Me NH Ph (CH₂)₂ Me Me C(═O)Me racemic VI-576 Me Me Me NH Ph (CH₂)₂ Me Me C(═O)Me (R)- VI-577 Me Et Me NH Ph (CH₂)₂ H H C(═O)Me racemic VI-578 Me Et Me NH Ph (CH₂)₂ H H C(═O)Me (R)- VI-579 Me Et Me NH Ph (CH₂)₂ Me H C(═O)Me racemic VI-580 Me Et Me NH Ph (CH₂)₂ Me H C(═O)Me (R)- VI-581 Me Et Me NH Ph (CH₂)₂ H Me C(═O)Me racemic VI-582 Me Et Me NH Ph (CH₂)₂ H Me C(═O)Me (R)- VI-583 Me Et Me NH Ph (CH₂)₂ Me Me C(═O)Me racemic VI-584 Me Et Me NH Ph (CH₂)₂ Me Me C(═O)Me (R)- VI-585 Me Me Me NH Ph (CH₂)₂ H H C(═O)Et racemic VI-586 Me Me Me NH Ph (CH₂)₂ H H C(═O)Et (R)- VI-587 Me Me Me NH Ph (CH₂)₂ Me H C(═O)Et racemic VI-588 Me Me Me NH Ph (CH₂)₂ Me H C(═O)Et (R)- VI-589 Me Me Me NH Ph (CH₂)₂ H Me C(═O)Et racemic VI-590 Me Me Me NH Ph (CH₂)₂ H Me C(═O)Et (R)- VI-591 Me Me Me NH Ph (CH₂)₂ Me Me C(═O)Et racemic VI-592 Me Me Me NH Ph (CH₂)₂ Me Me C(═O)Et (R)- VI-593 Me Et Me NH Ph (CH₂)₂ H H C(═O)Et racemic VI-594 Me Et Me NH Ph (CH₂)₂ H H C(═O)Et (R)- VI-595 Me Et Me NH Ph (CH₂)₂ Me H C(═O)Et racemic VI-596 Me Et Me NH Ph (CH₂)₂ Me H C(═O)Et (R)- VI-597 Me Et Me NH Ph (CH₂)₂ H Me C(═O)Et racemic VI-598 Me Et Me NH Ph (CH₂)₂ H Me C(═O)Et (R)- VI-599 Me Et Me NH Ph (CH₂)₂ Me Me C(═O)Et racemic VI-600 Me Et Me NH Ph (CH₂)₂ Me Me C(═O)Et (R)- VI-601 Me Me Me — Ph — H H Me racemic VI-602 Me Me Me — Ph — H H Me (R)- VI-603 Me Me Me — Ph — Me H Me racemic

TABLE 149 (VIa)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ uration VI-604 Me Me Me — Ph — Me H Me (R)- VI-605 Me Me Me — Ph — H Me Me racemic VI-606 Me Me Me — Ph — H Me Me (R)- VI-607 Me Me Me — Ph — Me Me Me racemic VI-608 Me Me Me — Ph — Me Me Me (R)- VI-609 Me Et Me — Ph — H H Me racemic VI-610 Me Et Me — Ph — H H Me (R)- VI-611 Me Et Me — Ph — Me H Me racemic VI-612 Me Et Me — Ph — Me H Me (R)- VI-613 Me Et Me — Ph — H Me Me racemic VI-614 Me Et Me — Ph — H Me Me (R)- VI-615 Me Et Me — Ph — Me Me Me racemic VI-616 Me Et Me — Ph — Me Me Me (R)- VI-617 Me Me Me — Ph — H H C(═O)Me racemic VI-618 Me Me Me — Ph — H H C(═O)Me (R)- VI-619 Me Me Me — Ph — Me H C(═O)Me racemic VI-620 Me Me Me — Ph — Me H C(═O)Me (R)- VI-621 Me Me Me — Ph — H Me C(═O)Me racemic VI-622 Me Me Me — Ph — H Me C(═O)Me (R)- VI-623 Me Me Me — Ph — Me Me C(═O)Me racemic VI-624 Me Me Me — Ph — Me Me C(═O)Me (R)- VI-625 Me Et Me — Ph — H H C(═O)Me racemic VI-626 Me Et Me — Ph — H H C(═O)Me (R)- VI-627 Me Et Me — Ph — Me H C(═O)Me racemic VI-628 Me Et Me — Ph — Me H C(═O)Me (R)- VI-629 Me Et Me — Ph — H Me C(═O)Me racemic VI-630 Me Et Me — Ph — H Me C(═O)Me (R)- VI-631 Me Et Me — Ph — Me Me C(═O)Me racemic VI-632 Me Et Me — Ph — Me Me C(═O)Me (R)- VI-633 Me Me Me — Ph — H H C(═O)Et racemic VI-634 Me Me Me — Ph — H H C(═O)Et (R)- VI-635 Me Me Me — Ph — Me H C(═O)Et racemic VI-636 Me Me Me — Ph — Me H C(═O)Et (R)- VI-637 Me Me Me — Ph — H Me C(═O)Et racemic VI-638 Me Me Me — Ph — H Me C(═O)Et (R)- VI-639 Me Me Me — Ph — Me Me C(═O)Et racemic VI-640 Me Me Me — Ph — Me Me C(═O)Et (R)- VI-641 Me Et Me — Ph — H H C(═O)Et racemic VI-642 Me Et Me — Ph — H H C(═O)Et (R)- VI-643 Me Et Me — Ph — Me H C(═O)Et racemic VI-644 Me Et Me — Ph — Me H C(═O)Et (R)- VI-645 Me Et Me — Ph — H Me C(═O)Et racemic VI-646 Me Et Me — Ph — H Me C(═O)Et (R)- VI-647 Me Et Me — Ph — Me Me C(═O)Et racemic VI-648 Me Et Me — Ph — Me Me C(═O)Et (R)- VI-649 Me Me Me — Ph CH₂ H H Me racemic VI-650 Me Me Me — Ph CH₂ H H Me (S)- VI-651 Me Me Me — Ph CH₂ Me H Me racemic VI-652 Me Me Me — Ph CH₂ Me H Me (S)- VI-653 Me Me Me — Ph CH₂ H Me Me racemic

TABLE 15 (VIa)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ uration VI-654 Me Me Me — Ph CH₂ H Me Me (S)- VI-655 Me Me Me — Ph CH₂ Me Me Me racemic VI-656 Me Me Me — Ph CH₂ Me Me Me (S)- VI-657 Me Et Me — Ph CH₂ H H Me racemic VI-658 Me Et Me — Ph CH₂ H H Me (S)- VI-659 Me Et Me — Ph CH₂ Me H Me racemic VI-660 Me Et Me — Ph CH₂ Me H Me (S)- VI-661 Me Et Me — Ph CH₂ H Me Me racemic VI-662 Me Et Me — Ph CH₂ H Me Me (S)- VI-663 Me Et Me — Ph CH₂ Me Me Me racemic VI-664 Me Et Me — Ph CH₂ Me Me Me (S)- VI-665 Me Me Me — Ph CH₂ H H C(═O)Me racemic VI-666 Me Me Me — Ph CH₂ H H C(═O)Me (S)- VI-667 Me Me Me — Ph CH₂ Me H C(═O)Me racemic VI-668 Me Me Me — Ph CH₂ Me H C(═O)Me (S)- VI-669 Me Me Me — Ph CH₂ H Me C(═O)Me racemic VI-670 Me Me Me — Ph CH₂ H Me C(═O)Me (S)- VI-671 Me Me Me — Ph CH₂ Me Me C(═O)Me racemic VI-672 Me Me Me — Ph CH₂ Me Me C(═O)Me (S)- VI-673 Me Et Me — Ph CH₂ H H C(═O)Me racemic VI-674 Me Et Me — Ph CH₂ H H C(═O)Me (S)- VI-675 Me Et Me — Ph CH₂ Me H C(═O)Me racemic VI-676 Me Et Me — Ph CH₂ Me H C(═O)Me (S)- VI-677 Me Et Me — Ph CH₂ H Me C(═O)Me racemic VI-678 Me Et Me — Ph CH₂ H Me C(═O)Me (S)- VI-679 Me Et Me — Ph CH₂ Me Me C(═O)Me racemic VI-680 Me Et Me — Ph CH₂ Me Me C(═O)Me (S)- VI-681 Me Me Me — Ph CH₂ H H C(═O)Et racemic VI-682 Me Me Me — Ph CH₂ H H C(═O)Et (S)- VI-683 Me Me Me — Ph CH₂ Me H C(═O)Et racemic VI-684 Me Me Me — Ph CH₂ Me H C(═O)Et (S)- VI-685 Me Me Me — Ph CH₂ H Me C(═O)Et racemic VI-686 Me Me Me — Ph CH₂ H Me C(═O)Et (S)- VI-687 Me Me Me — Ph CH₂ Me Me C(═O)Et racemic VI-688 Me Me Me — Ph CH₂ Me Me C(═O)Et (S)- VI-689 Me Et Me — Ph CH₂ H H C(═O)Et racemic VI-690 Me Et Me — Ph CH₂ H H C(═O)Et (S)- VI-691 Me Et Me — Ph CH₂ Me H C(═O)Et racemic VI-692 Me Et Me — Ph CH₂ Me H C(═O)Et (S)- VI-693 Me Et Me — Ph CH₂ H Me C(═O)Et racemic VI-694 Me Et Me — Ph CH₂ H Me C(═O)Et (S)- VI-695 Me Et Me — Ph CH₂ Me Me C(═O)Et racemic VI-696 Me Et Me — Ph CH₂ Me Me C(═O)Et (S)-

TABLE 151 (VIb)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ uration VI-177 Me Me Me O Ph CH₂ H H Me racemic VI-178 Me Me Me O Ph CH₂ H H Me (S)- VI-179 Me Me Me O Ph CH₂ Me H Me racemic VI-180 Me Me Me O Ph CH₂ Me H Me (S)- VI-181 Me Me Me O Ph CH₂ H Me Me racemic VI-182 Me Me Me O Ph CH₂ H Me Me (S)- VI-183 Me Me Me O Ph CH₂ Me Me Me racemic VI-184 Me Me Me O Ph CH₂ Me Me Me (S)- VI-185 Me Et Me O Ph CH₂ H H Me racemic VI-186 Me Et Me O Ph CH₂ H H Me (S)- VI-187 Me Et Me O Ph CH₂ Me H Me racemic VI-188 Me Et Me O Ph CH₂ Me H Me (S)- VI-189 Me Et Me O Ph CH₂ H Me Me racemic VI-190 Me Et Me O Ph CH₂ H Me Me (S)- VI-191 Me Et Me O Ph CH₂ Me Me Me racemic VI-192 Me Et Me O Ph CH₂ Me Me Me (S)- VI-193 Me Me Me O Ph CH₂ H H Et racemic VI-194 Me Me Me O Ph CH₂ H H Et (S)- VI-195 Me Me Me O Ph CH₂ Me H Et racemic VI-196 Me Me Me O Ph CH₂ Me H Et (S)- VI-197 Me Me Me O Ph CH₂ H Me Et racemic VI-198 Me Me Me O Ph CH₂ H Me Et (S)- VI-199 Me Me Me O Ph CH₂ Me Me Et racemic VI-200 Me Me Me O Ph CH₂ Me Me Et (S)- VI-201 Me Et Me O Ph CH₂ H H Et racemic VI-202 Me Et Me O Ph CH₂ H H Et (S)- VI-203 Me Et Me O Ph CH₂ Me H Et racemic VI-204 Me Et Me O Ph CH₂ Me H Et (S)- VI-205 Me Et Me O Ph CH₂ H Me Et racemic VI-206 Me Et Me O Ph CH₂ H Me Et (S)- VI-207 Me Et Me O Ph CH₂ Me Me Et racemic VI-208 Me Et Me O Ph CH₂ Me Me Et (S)- VI-209 Me Me Me NH Ph CH₂ H H Me racemic VI-210 Me Me Me NH Ph CH₂ H H Me (S)- VI-211 Me Me Me NH Ph CH₂ Me H Me racemic VI-212 Me Me Me NH Ph CH₂ Me H Me (S)- VI-213 Me Me Me NH Ph CH₂ H Me Me racemic VI-214 Me Me Me NH Ph CH₂ H Me Me (S)- VI-215 Me Me Me NH Ph CH₂ Me Me Me racemic VI-216 Me Me Me NH Ph CH₂ Me Me Me (S)- VI-217 Me Et Me NH Ph CH₂ H H Me racemic VI-218 Me Et Me NH Ph CH₂ H H Me (S)- VI-219 Me Et Me NH Ph CH₂ Me H Me racemic VI-220 Me Et Me NH Ph CH₂ Me H Me (S)- VI-221 Me Et Me NH Ph CH₂ H Me Me racemic VI-222 Me Et Me NH Ph CH₂ H Me Me (S)- VI-223 Me Et Me NH Ph CH₂ Me Me Me racemic VI-224 Me Et Me NH Ph CH₂ Me Me Me (S)- VI-225 Me Me Me NH Ph CH₂ H H Et racemic VI-226 Me Me Me NH Ph CH₂ H H Et (S)-

TABLE 152 (VIb)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ uration VI-227 Me Me Me NH Ph CH₂ Me H Et racemic VI-228 Me Me Me NH Ph CH₂ Me H Et (S)- VI-229 Me Me Me NH Ph CH₂ H Me Et racemic VI-230 Me Me Me NH Ph CH₂ H Me Et (S)- VI-231 Me Me Me NH Ph CH₂ Me Me Et racemic VI-232 Me Me Me NH Ph CH₂ Me Me Et (S)- VI-233 Me Et Me NH Ph CH₂ H H Et racemic VI-234 Me Et Me NH Ph CH₂ H H Et (S)- VI-235 Me Et Me NH Ph CH₂ Me H Et racemic VI-236 Me Et Me NH Ph CH₂ Me H Et (S)- VI-237 Me Et Me NH Ph CH₂ H Me Et racemic VI-238 Me Et Me NH Ph CH₂ H Me Et (S)- VI-239 Me Et Me NH Ph CH₂ Me Me Et racemic VI-240 Me Et Me NH Ph CH₂ Me Me Et (S)- VI-241 Me Me Me NH Ph CH₂ H H C(═O)Me racemic VI-242 Me Me Me NH Ph CH₂ H H C(═O)Me (S)- VI-243 Me Me Me NH Ph CH₂ Me H C(═O)Me racemic VI-244 Me Me Me NH Ph CH₂ Me H C(═O)Me (S)- VI-245 Me Me Me NH Ph CH₂ H Me C(═O)Me racemic VI-246 Me Me Me NH Ph CH₂ H Me C(═O)Me (S)- VI-247 Me Me Me NH Ph CH₂ Me Me C(═O)Me racemic VI-248 Me Me Me NH Ph CH₂ Me Me C(═O)Me (S)- VI-249 Me Et Me NH Ph CH₂ H H C(═O)Me racemic VI-250 Me Et Me NH Ph CH₂ H H C(═O)Me (S)- VI-251 Me Et Me NH Ph CH₂ Me H C(═O)Me racemic VI-252 Me Et Me NH Ph CH₂ Me H C(═O)Me (S)- VI-253 Me Et Me NH Ph CH₂ H Me C(═O)Me racemic VI-254 Me Et Me NH Ph CH₂ H Me C(═O)Me (S)- VI-255 Me Et Me NH Ph CH₂ Me Me C(═O)Me racemic VI-256 Me Et Me NH Ph CH₂ Me Me C(═O)Me (S)- VI-257 Me Me Me NH Ph CH₂ H H C(═O)Et racemic VI-258 Me Me Me NH Ph CH₂ H H C(═O)Et (S)- VI-259 Me Me Me NH Ph CH₂ Me H C(═O)Et racemic VI-260 Me Me Me NH Ph CH₂ Me H C(═O)Et (S)- VI-261 Me Me Me NH Ph CH₂ H Me C(═O)Et racemic VI-262 Me Me Me NH Ph CH₂ H Me C(═O)Et (S)- VI-263 Me Me Me NH Ph CH₂ Me Me C(═O)Et racemic VI-264 Me Me Me NH Ph CH₂ Me Me C(═O)Et (S)- VI-265 Me Et Me NH Ph CH₂ H H C(═O)Et racemic VI-266 Me Et Me NH Ph CH₂ H H C(═O)Et (S)- VI-267 Me Et Me NH Ph CH₂ Me H C(═O)Et racemic VI-268 Me Et Me NH Ph CH₂ Me H C(═O)Et (S)- VI-269 Me Et Me NH Ph CH₂ H Me C(═O)Et racemic VI-270 Me Et Me NH Ph CH₂ H Me C(═O)Et (S)- VI-271 Me Et Me NH Ph CH₂ Me Me C(═O)Et racemic VI-272 Me Et Me NH Ph CH₂ Me Me C(═O)Et (S)- VI-273 Me Me Me NH Ph CH₂ H H C(═O)tBu racemic VI-274 Me Me Me NH Ph CH₂ H H C(═O)tBu (S)- VI-275 Me Me Me NH Ph CH₂ Me H C(═O)tBu racemic VI-276 Me Me Me NH Ph CH₂ Me H C(═O)tBu (S)-

TABLE 153 (VIb)

Compound No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ Configuration VI-277 Me Me Me NH Ph CH₂ H Me C(═O)tBu racemic VI-278 Me Me Me NH Ph CH₂ H Me C(═O)tBu (S)- VI-279 Me Me Me NH Ph CH₂ Me Me C(═O)tBu racemic VI-280 Me Me Me NH Ph CH₂ Me Me C(═O)tBu (S)- VI-281 Me Et Me NH Ph CH₂ H H C(═O)tBu racemic VI-282 Me Et Me NH Ph CH₂ H H C(═O)tBu (S)- VI-283 Me Et Me NH Ph CH₂ Me H C(═O)tBu racemic VI-284 Me Et Me NH Ph CH₂ Me H C(═O)tBu (S)- VI-285 Me Et Me NH Ph CH₂ H Me C(═O)tBu racemic VI-286 Me Et Me NH Ph CH₂ H Me C(═O)tBu (S)- VI-287 Me Et Me NH Ph CH₂ Me Me C(═O)tBu racemic VI-288 Me Et Me NH Ph CH₂ Me Me C(═O)tBu (S)- VI-289 Me Me Me NH Ph CH₂ H H C(═O)OEt racemic VI-290 Me Me Me NH Ph CH₂ H H C(═O)OEt (S)- VI-291 Me Me Me NH Ph CH₂ Me H C(═O)OEt racemic VI-292 Me Me Me NH Ph CH₂ Me H C(═O)OEt (S)- VI-293 Me Me Me NH Ph CH₂ H Me C(═O)OEt racemic VI-294 Me Me Me NH Ph CH₂ H Me C(═O)OEt (S)- VI-295 Me Me Me NH Ph CH₂ Me Me C(═O)OEt racemic VI-296 Me Me Me NH Ph CH₂ Me Me C(═O)OEt (S)- VI-297 Me Et Me NH Ph CH₂ H H C(═O)OEt racemic VI-298 Me Et Me NH Ph CH₂ H H C(═O)OEt (S)- VI-299 Me Et Me NH Ph CH₂ Me H C(═O)OEt racemic VI-300 Me Et Me NH Ph CH₂ Me H C(═O)OEt (S)- VI-301 Me Et Me NH Ph CH₂ H Me C(═O)OEt racemic VI-302 Me Et Me NH Ph CH₂ H Me C(═O)OEt (S)- VI-303 Me Et Me NH Ph CH₂ Me Me C(═O)OEt racemic VI-304 Me Et Me NH Ph CH₂ Me Me C(═O)OEt (S)- VI-305 Me Me Me NH Ph CH₂ H H C(═O)OcHex racemic VI-306 Me Me Me NH Ph CH₂ H H C(═O)OcHex (S)- VI-307 Me Me Me NH Ph CH₂ Me H C(═O)OcHex Hracemic VI-308 Me Me Me NH Ph CH₂ Me H C(═O)OcHex (S)- VI-309 Me Me Me NH Ph CH₂ H Me C(═O)OcHex racemic VI-310 Me Me Me NH Ph CH₂ H Me C(═O)OcHex (S)- VI-311 Me Me Me NH Ph CH₂ Me Me C(═O)OcHex racemic VI-312 Me Me Me NH Ph CH₂ Me Me C(═O)OcHex (S)- VI-313 Me Et Me NH Ph CH₂ H H C(═O)OcHex racemic VI-314 Me Et Me NH Ph CH₂ H H C(═O)OcHex (S)- VI-315 Me Et Me NH Ph CH₂ Me H C(═O)OcHex racemic VI-316 Me Et Me NH Ph CH₂ Me H C(═O)OcHex (S)- VI-317 Me Et Me NH Ph CH₂ H Me C(═O)OcHex racemic VI-318 Me Et Me NH Ph CH₂ H Me C(═O)OcHex (S)- VI-319 Me Et Me NH Ph CH₂ Me Me C(═O)OcHex racemic VI-320 Me Et Me NH Ph CH₂ Me Me C(═O)OcHex (S)- VI-321 Me Me Me CH₂ Ph CH₂ H H Me racemic VI-322 Me Me Me CH₂ Ph CH₂ H H Me (S)- VI-323 Me Me Me CH₂ Ph CH₂ Me H Me racemic VI-324 Me Me Me CH₂ Ph CH₂ Me H Me (S)- VI-325 Me Me Me CH₂ Ph CH₂ H Me Me racemic VI-326 Me Me Me CH₂ Ph CH₂ H Me Me (S)-

TABLE 154 (VIb)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ uration VI-327 Me Me Me CH₂ Ph CH₂ Me Me Me racemic VI-328 Me Me Me CH₂ Ph CH₂ Me Me Me (S)- VI-329 Me Et Me CH₂ Ph CH₂ H H Me racemic VI-330 Me Et Me CH₂ Ph CH₂ H H Me (S)- VI-331 Me Et Me CH₂ Ph CH₂ Me H Me racemic VI-332 Me Et Me CH₂ Ph CH₂ Me H Me (S)- VI-333 Me Et Me CH₂ Ph CH₂ H Me Me racemic VI-334 Me Et Me CH₂ Ph CH₂ H Me Me (S)- VI-335 Me Et Me CH₂ Ph CH₂ Me Me Me racemic VI-336 Me Et Me CH₂ Ph CH₂ Me Me Me (S)- VI-337 Me Me Me CH₂ Ph CH₂ H H Et racemic VI-338 Me Me Me CH₂ Ph CH₂ H H Et (S)- VI-339 Me Me Me CH₂ Ph CH₂ Me H Et racemic VI-340 Me Me Me CH₂ Ph CH₂ Me H Et (S)- VI-341 Me Me Me CH₂ Ph CH₂ H Me Et racemic VI-342 Me Me Me CH₂ Ph CH₂ H Me Et (S)- VI-343 Me Me Me CH₂ Ph CH₂ Me Me Et racemic VI-344 Me Me Me CH₂ Ph CH₂ Me Me Et (S)- VI-345 Me Et Me CH₂ Ph CH₂ H H Et racemic VI-346 Me Et Me CH₂ Ph CH₂ H H Et (S)- VI-347 Me Et Me CH₂ Ph CH₂ Me H Et racemic VI-348 Me Et Me CH₂ Ph CH₂ Me H Et (S)- VI-349 Me Et Me CH₂ Ph CH₂ H Me Et racemic VI-350 Me Et Me CH₂ Ph CH₂ H Me Et (S)- VI-351 Me Et Me CH₂ Ph CH₂ Me Me Et racemic VI-352 Me Et Me CH₂ Ph CH₂ Me Me Et (S)-

TABLE 155 (VIb)

Com- Config- pound No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ uration VI-697 Me Me Me NH Ph (CH₂)₂ H H Me racemic VI-698 Me Me Me NH Ph (CH₂)₂ H H Me (R)- VI-699 Me Me Me NH Ph (CH₂)₂ Me H Me racemic VI-700 Me Me Me NH Ph (CH₂)₂ Me H Me (R)- VI-701 Me Me Me NH Ph (CH₂)₂ H Me Me racemic VI-702 Me Me Me NH Ph (CH₂)₂ H Me Me (R)- VI-703 Me Me Me NH Ph (CH₂)₂ Me Me Me racemic VI-704 Me Me Me NH Ph (CH₂)₂ Me Me Me (R)- VI-705 Me Et Me NH Ph (CH₂)₂ H H Me racemic VI-706 Me Et Me NH Ph (CH₂)₂ H H Me (R)- VI-707 Me Et Me NH Ph (CH₂)₂ Me H Me racemic VI-708 Me Et Me NH Ph (CH₂)₂ Me H Me (R)- VI-709 Me Et Me NH Ph (CH₂)₂ H Me Me racemic VI-710 Me Et Me NH Ph (CH₂)₂ H Me Me (R)- VI-711 Me Et Me NH Ph (CH₂)₂ Me Me Me racemic VI-712 Me Et Me NH Ph (CH₂)₂ Me Me Me (R)- VI-713 Me Me Me NH Ph (CH₂)₂ H H C(═O)Me racemic VI-714 Me Me Me NH Ph (CH₂)₂ H H C(═O)Me (R)- VI-715 Me Me Me NH Ph (CH₂)₂ Me H C(═O)Me racemic VI-716 Me Me Me NH Ph (CH₂)₂ Me H C(═O)Me (R)- VI-717 Me Me Me NH Ph (CH₂)₂ H Me C(═O)Me racemic VI-718 Me Me Me NH Ph (CH₂)₂ H Me C(═O)Me (R)- VI-719 Me Me Me NH Ph (CH₂)₂ Me Me C(═O)Me racemic VI-720 Me Me Me NH Ph (CH₂)₂ Me Me C(═O)Me (R)- VI-721 Me Et Me NH Ph (CH₂)₂ H H C(═O)Me racemic VI-722 Me Et Me NH Ph (CH₂)₂ H H C(═O)Me (R)- VI-723 Me Et Me NH Ph (CH₂)₂ Me H C(═O)Me racemic VI-724 Me Et Me NH Ph (CH₂)₂ Me H C(═O)Me (R)- VI-725 Me Et Me NH Ph (CH₂)₂ H Me C(═O)Me racemic VI-726 Me Et Me NH Ph (CH₂)₂ H Me C(═O)Me (R)- VI-727 Me Et Me NH Ph (CH₂)₂ Me Me C(═O)Me racemic VI-728 Me Et Me NH Ph (CH₂)₂ Me Me C(═O)Me (R)- VI-729 Me Me Me NH Ph (CH₂)₂ H H C(═O)Et racemic VI-730 Me Me Me NH Ph (CH₂)₂ H H C(═O)Et (R)- VI-731 Me Me Me NH Ph (CH₂)₂ Me H C(═O)Et racemic VI-732 Me Me Me NH Ph (CH₂)₂ Me H C(═O)Et (R)- VI-733 Me Me Me NH Ph (CH₂)₂ H Me C(═O)Et racemic VI-734 Me Me Me NH Ph (CH₂)₂ H Me C(═O)Et (R)- VI-735 Me Me Me NH Ph (CH₂)₂ Me Me C(═O)Et racemic VI-736 Me Me Me NH Ph (CH₂)₂ Me Me C(═O)Et (R)- VI-737 Me Et Me NH Ph (CH₂)₂ H H C(═O)Et racemic VI-738 Me Et Me NH Ph (CH₂)₂ H H C(═O)Et (R)- VI-739 Me Et Me NH Ph (CH₂)₂ Me H C(═O)Et racemic VI-740 Me Et Me NH Ph (CH₂)₂ Me H C(═O)Et (R)- VI-741 Me Et Me NH Ph (CH₂)₂ H Me C(═O)Et racemic VI-742 Me Et Me NH Ph (CH₂)₂ H Me C(═O)Et (R)- VI-743 Me Et Me NH Ph (CH₂)₂ Me Me C(═O)Et racemic VI-744 Me Et Me NH Ph (CH₂)₂ Me Me C(═O)Et (R)- VI-745 Me Me Me — Ph — H H Me racemic VI-746 Me Me Me — Ph — H H Me (R)-

TABLE 156 (VIb)

Com- pound Con- No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ figuration VI-747 Me Me Me — Ph — Me H Me racemic VI-748 Me Me Me — Ph — Me H Me (R)- VI-749 Me Me Me — Ph — H Me Me racemic VI-750 Me Me Me — Ph — H Me Me (R)- VI-751 Me Me Me — Ph — Me Me Me racemic VI-752 Me Me Me — Ph — Me Me Me (R)- VI-753 Me Et Me — Ph — H H Me racemic VI-754 Me Et Me — Ph — H H Me (R)- VI-755 Me Et Me — Ph — Me H Me racemic VI-756 Me Et Me — Ph — Me H Me (R)- VI-757 Me Et Me — Ph — H Me Me racemic VI-758 Me Et Me — Ph — H Me Me (R)- VI-759 Me Et Me — Ph — Me Me Me racemic VI-760 Me Et Me — Ph — Me Me Me (R)- VI-761 Me Me Me — Ph — H H C(═O)Me racemic VI-762 Me Me Me — Ph — H H C(═O)Me (R)- VI-763 Me Me Me — Ph — Me H C(═O)Me racemic VI-764 Me Me Me — Ph — Me H C(═O)Me (R)- VI-765 Me Me Me — Ph — H Me C(═O)Me racemic VI-766 Me Me Me — Ph — H Me C(═O)Me (R)- VI-767 Me Me Me — Ph — Me Me C(═O)Me racemic VI-768 Me Me Me — Ph — Me Me C(═O)Me (R)- VI-769 Me Et Me — Ph — H H C(═O)Me racemic VI-770 Me Et Me — Ph — H H C(═O)Me (R)- VI-771 Me Et Me — Ph — Me H C(═O)Me racemic VI-772 Me Et Me — Ph — Me H C(═O)Me (R)- VI-773 Me Et Me — Ph — H Me C(═O)Me racemic VI-774 Me Et Me — Ph — H Me C(═O)Me (R)- VI-775 Me Et Me — Ph — Me Me C(═O)Me racemic VI-776 Me Et Me — Ph — Me Me C(═O)Me (R)- VI-777 Me Me Me — Ph — H H C(═O)Et racemic VI-778 Me Me Me — Ph — H H C(═O)Et (R)- VI-779 Me Me Me — Ph — Me H C(═O)Et racemic VI-780 Me Me Me — Ph — Me H C(═O)Et (R)- VI-781 Me Me Me — Ph — H Me C(═O)Et racemic VI-782 Me Me Me — Ph — H Me C(═O)Et (R)- VI-783 Me Me Me — Ph — Me Me C(═O)Et racemic VI-784 Me Me Me — Ph — Me Me C(═O)Et (R)- VI-785 Me Et Me — Ph — H H C(═O)Et racemic VI-786 Me Et Me — Ph — H H C(═O)Et (R)- VI-787 Me Et Me — Ph — Me H C(═O)Et racemic VI-788 Me Et Me — Ph — Me H C(═O)Et (R)- VI-789 Me Et Me — Ph — H Me C(═O)Et racemic VI-790 Me Et Me — Ph — H Me C(═O)Et (R)- VI-791 Me Et Me — Ph — Me Me C(═O)Et racemic VI-792 Me Et Me — Ph — Me Me C(═O)Et (R)- VI-793 Me Me Me — Ph CH₂ H H Me racemic VI-794 Me Me Me — Ph CH₂ H H Me (S)- VI-795 Me Me Me — Ph CH₂ Me H Me racemic VI-796 Me Me Me — Ph CH₂ Me H Me (S)-

TABLE 157 (VIb)

Com- pound Con- No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ figuration VI-797 Me Me Me — Ph CH₂ H Me Me racemic VI-798 Me Me Me — Ph CH₂ H Me Me (S)- VI-799 Me Me Me — Ph CH₂ Me Me Me racemic VI-800 Me Me Me — Ph CH₂ Me Me Me (S)- VI-801 Me Et Me — Ph CH₂ H H Me racemic VI-802 Me Et Me — Ph CH₂ H H Me (S)- VI-803 Me Et Me — Ph CH₂ Me H Me racemic VI-804 Me Et Me — Ph CH₂ Me H Me (S)- VI-805 Me Et Me — Ph CH₂ H Me Me racemic VI-806 Me Et Me — Ph CH₂ H Me Me (S)- VI-807 Me Et Me — Ph CH₂ Me Me Me racemic VI-808 Me Et Me — Ph CH₂ Me Me Me (S)- VI-809 Me Me Me — Ph CH₂ H H C(═O)Me racemic VI-810 Me Me Me — Ph CH₂ H H C(═O)Me (S)- VI-811 Me Me Me — Ph CH₂ Me H C(═O)Me racemic VI-812 Me Me Me — Ph CH₂ Me H C(═O)Me (S)- VI-813 Me Me Me — Ph CH₂ H Me C(═O)Me racemic VI-814 Me Me Me — Ph CH₂ H Me C(═O)Me (S)- VI-815 Me Me Me — Ph CH₂ Me Me C(═O)Me racemic VI-816 Me Me Me — Ph CH₂ Me Me C(═O)Me (S)- VI-817 Me Et Me — Ph CH₂ H H C(═O)Me racemic VI-818 Me Et Me — Ph CH₂ H H C(═O)Me (S)- VI-819 Me Et Me — Ph CH₂ Me H C(═O)Me racemic VI-820 Me Et Me — Ph CH₂ Me H C(═O)Me (S)- VI-821 Me Et Me — Ph CH₂ H Me C(═O)Me racemic VI-822 Me Et Me — Ph CH₂ H Me C(═O)Me (S)- VI-823 Me Et Me — Ph CH₂ Me Me C(═O)Me racemic VI-824 Me Et Me — Ph CH₂ Me Me C(═O)Me (S)- VI-825 Me Me Me — Ph CH₂ H H C(═O)Et racemic VI-826 Me Me Me — Ph CH₂ H H C(═O)Et (S)- VI-827 Me Me Me — Ph CH₂ Me H C(═O)Et racemic VI-828 Me Me Me — Ph CH₂ Me H C(═O)Et (S)- VI-829 Me Me Me — Ph CH₂ H Me C(═O)Et racemic VI-830 Me Me Me — Ph CH₂ H Me C(═O)Et (S)- VI-831 Me Me Me — Ph CH₂ Me Me C(═O)Et racemic VI-832 Me Me Me — Ph CH₂ Me Me C(═O)Et (S)- VI-833 Me Et Me — Ph CH₂ H H C(═O)Et racemic VI-834 Me Et Me — Ph CH₂ H H C(═O)Et (S)- VI-835 Me Et Me — Ph CH₂ Me H C(═O)Et racemic VI-836 Me Et Me — Ph CH₂ Me H C(═O)Et (S)- VI-837 Me Et Me — Ph CH₂ H Me C(═O)Et racemic VI-838 Me Et Me — Ph CH₂ H Me C(═O)Et (S)- VI-839 Me Et Me — Ph CH₂ Me Me C(═O)Et racemic VI-840 Me Et Me — Ph CH₂ Me Me C(═O)Et (S)-

TABLE 158 (VIc)

Compound No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ Configuration VI-353 Me Me Me O Ph CH₂ H H Me racemic VI-354 Me Me Me O Ph CH₂ H H Me (S)- VI-355 Me Me Me O Ph CH₂ Me H Me racemic VI-356 Me Me Me O Ph CH₂ Me H Me (S)- VI-357 Me Me Me O Ph CH₂ H Me Me racemic VI-358 Me Me Me O Ph CH₂ H Me Me (S)- VI-359 Me Me Me O Ph CH₂ Me Me Me racemic VI-360 Me Me Me O Ph CH₂ Me Me Me (S)- VI-361 Me Et Me O Ph CH₂ H H Me racemic VI-362 Me Et Me O Ph CH₂ H H Me (S)- VI-363 Me Et Me O Ph CH₂ Me H Me racemic VI-364 Me Et Me O Ph CH₂ Me H Me (S)- VI-365 Me Et Me O Ph CH₂ H Me Me racemic VI-366 Me Et Me O Ph CH₂ H Me Me (S)- VI-367 Me Et Me O Ph CH₂ Me Me Me racemic VI-368 Me Et Me O Ph CH₂ Me Me Me (S)- VI-369 Me Me Me O Ph CH₂ H H Et racemic VI-370 Me Me Me O Ph CH₂ H H Et (S)- VI-371 Me Me Me O Ph CH₂ Me H Et racemic VI-372 Me Me Me O Ph CH₂ Me H Et (S)- VI-373 Me Me Me O Ph CH₂ H Me Et racemic VI-374 Me Me Me O Ph CH₂ H Me Et (S)- VI-375 Me Me Me O Ph CH₂ Me Me Et racemic VI-376 Me Me Me O Ph CH₂ Me Me Et (S)- VI-377 Me Et Me O Ph CH₂ H H Et racemic VI-378 Me Et Me O Ph CH₂ H H Et (S)- VI-379 Me Et Me O Ph CH₂ Me H Et racemic VI-380 Me Et Me O Ph CH₂ Me H Et (S)- VI-381 Me Et Me O Ph CH₂ H Me Et racemic VI-382 Me Et Me O Ph CH₂ H Me Et (S)- VI-383 Me Et Me O Ph CH₂ Me Me Et racemic VI-384 Me Et Me O Ph CH₂ Me Me Et (S)- VI-385 Me Me Me NH Ph CH₂ H H Me racemic VI-386 Me Me Me NH Ph CH₂ H H Me (S)- VI-387 Me Me Me NH Ph CH₂ Me H Me racemic VI-388 Me Me Me NH Ph CH₂ Me H Me (S)- VI-389 Me Me Me NH Ph CH₂ H Me Me racemic VI-390 Me Me Me NH Ph CH₂ H Me Me (S)- VI-391 Me Me Me NH Ph CH₂ Me Me Me racemic VI-392 Me Me Me NH Ph CH₂ Me Me Me (S)- VI-393 Me Et Me NH Ph CH₂ H H Me racemic VI-394 Me Et Me NH Ph CH₂ H H Me (S)- VI-395 Me Et Me NH Ph CH₂ Me H Me racemic VI-396 Me Et Me NH Ph CH₂ Me H Me (S)- VI-397 Me Et Me NH Ph CH₂ H Me Me racemic VI-398 Me Et Me NH Ph CH₂ H Me Me (S)- VI-399 Me Et Me NH Ph CH₂ Me Me Me racemic VI-400 Me Et Me NH Ph CH₂ Me Me Me (S)- VI-401 Me Me Me NH Ph CH₂ H H Et racemic VI-402 Me Me Me NH Ph CH₂ H H Et (S)-

TABLE 159 (VIc)

Com- Con- pound figu- No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ ration VI-403 Me Me Me NH Ph CH₂ Me H Et racemic VI-404 Me Me Me NH Ph CH₂ Me H Et (S)- VI-405 Me Me Me NH Ph CH₂ H Me Et racemic VI-406 Me Me Me NH Ph CH₂ H Me Et (S)- VI-407 Me Me Me NH Ph CH₂ Me Me Et racemic VI-408 Me Me Me NH Ph CH₂ Me Me Et (S)- VI-409 Me Et Me NH Ph CH₂ H H Et racemic VI-410 Me Et Me NH Ph CH₂ H H Et (S)- VI-411 Me Et Me NH Ph CH₂ Me H Et racemic VI-412 Me Et Me NH Ph CH₂ Me H Et (S)- VI-413 Me Et Me NH Ph CH₂ H Me Et racemic VI-414 Me Et Me NH Ph CH₂ H Me Et (S)- VI-415 Me Et Me NH Ph CH₂ Me Me Et racemic VI-416 Me Et Me NH Ph CH₂ Me Me Et (S)- VI-417 Me Me Me NH Ph CH₂ H H (5-Methyl-2- racemic oxo-1,3- dioxol-4-yl) methyl VI-418 Me Me Me NH Ph CH₂ H H (5-Methyl-2- (S)- oxo-1,3- dioxol-4-yl) methyl VI-419 Me Me Me NH Ph CH₂ Me H (5-Methyl-2- racemic oxo-1,3- dioxol-4-yl) methyl VI-420 Me Me Me NH Ph CH₂ Me H (5-Methyl-2- (S)- oxo-1,3- dioxol-4-yl) methyl VI-421 Me Me Me NH Ph CH₂ H Me (5-Methyl-2- racemic oxo-1,3- dioxol-4-yl) methyl VI-422 Me Me Me NH Ph CH₂ H Me (5-Methyl-2- (S)- oxo-1,3- dioxol-4-yl) methyl VI-423 Me Me Me NH Ph CH₂ Me Me (5-Methyl-2- racemic oxo-1,3- dioxol-4-yl) methyl VI-424 Me Me Me NH Ph CH₂ Me Me (5-Methyl-2- (S)- oxo-1,3- dioxol-4-yl) methyl VI-425 Me Me Me NH Ph CH₂ H H C(═O)H racemic VI-426 Me Me Me NH Ph CH₂ H H C(═O)H (S)- VI-427 Me Me Me NH Ph CH₂ Me H C(═O)H racemic VI-428 Me Me Me NH Ph CH₂ Me H C(═O)H (S)- VI-429 Me Me Me NH Ph CH₂ H Me C(═O)H racemic VI-430 Me Me Me NH Ph CH₂ H Me C(═O)H (S)- VI-431 Me Me Me NH Ph CH₂ Me Me C(═O)H racemic VI-432 Me Me Me NH Ph CH₂ Me Me C(═O)H (S)- VI-433 Me Et Me NH Ph CH₂ H H C(═O)H racemic VI-434 Me Et Me NH Ph CH₂ H H C(═O)H (S)- VI-435 Me Et Me NH Ph CH₂ Me H C(═O)H racemic VI-436 Me Et Me NH Ph CH₂ Me H C(═O)H (S)- VI-437 Me Et Me NH Ph CH₂ H Me C(═O)H racemic VI-438 Me Et Me NH Ph CH₂ H Me C(═O)H (S)- VI-439 Me Et Me NH Ph CH₂ Me Me C(═O)H racemic VI-440 Me Et Me NH Ph CH₂ Me Me C(═O)H (S)- VI-441 Me Me Me NH Ph CH₂ H H C(═O)Me racemic VI-442 Me Me Me NH Ph CH₂ H H C(═O)Me (S)- VI-443 Me Me Me NH Ph CH₂ Me H C(═O)Me racemic VI-444 Me Me Me NH Ph CH₂ Me H C(═O)Me (S)- VI-445 Me Me Me NH Ph CH₂ H Me C(═O)Me racemic VI-446 Me Me Me NH Ph CH₂ H Me C(═O)Me (S)- VI-447 Me Me Me NH Ph CH₂ Me Me C(═O)Me racemic VI-448 Me Me Me NH Ph CH₂ Me Me C(═O)Me (S)- VI-449 Me Et Me NH Ph CH₂ H H C(═O)Me racemic VI-450 Me Et Me NH Ph CH₂ H H C(═O)Me (S)- VI-451 Me Et Me NH Ph CH₂ Me H C(═O)Me racemic VI-452 Me Et Me NH Ph CH₂ Me H C(═O)Me (S)-

TABLE 160 (VIc)

Com- pound Con- No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ figuration VI-453 Me Et Me NH Ph CH₂ H Me C(═O)Me racemic VI-454 Me Et Me NH Ph CH₂ H Me C(═O)Me (S)- VI-455 Me Et Me NH Ph CH₂ Me Me C(═O)Me racemic VI-456 Me Et Me NH Ph CH₂ Me Me C(═O)Me (S)- VI-457 Me Me Me NH Ph CH₂ H H C(═O)Et racemic VI-458 Me Me Me NH Ph CH₂ H H C(═O)Et (S)- VI-459 Me Me Me NH Ph CH₂ Me H C(═O)Et racemic VI-460 Me Me Me NH Ph CH₂ Me H C(═O)Et (S)- VI-461 Me Me Me NH Ph CH₂ H Me C(═O)Et racemic VI-462 Me Me Me NH Ph CH₂ H Me C(═O)Et (S)- VI-463 Me Me Me NH Ph CH₂ Me Me C(═O)Et racemic VI-464 Me Me Me NH Ph CH₂ Me Me C(═O)Et (S)- VI-465 Me Et Me NH Ph CH₂ H H C(═O)Et racemic VI-466 Me Et Me NH Ph CH₂ H H C(═O)Et (S)- VI-467 Me Et Me NH Ph CH₂ Me H C(═O)Et racemic VI-468 Me Et Me NH Ph CH₂ Me H C(═O)Et (S)- VI-469 Me Et Me NH Ph CH₂ H Me C(═O)Et racemic VI-470 Me Et Me NH Ph CH₂ H Me C(═O)Et (S)- VI-471 Me Et Me NH Ph CH₂ Me Me C(═O)Et racemic VI-472 Me Et Me NH Ph CH₂ Me Me C(═O)Et (S)- VI-473 Me Me Me NH Ph CH₂ H H C(═O)tBu racemic VI-474 Me Me Me NH Ph CH₂ H H C(═O)tBu (S)- VI-475 Me Me Me NH Ph CH₂ Me H C(═O)tBu racemic VI-476 Me Me Me NH Ph CH₂ Me H C(═O)tBu (S)- VI-477 Me Me Me NH Ph CH₂ H Me C(═O)tBu racemic VI-478 Me Me Me NH Ph CH₂ H Me C(═O)tBu (S)- VI-479 Me Me Me NH Ph CH₂ Me Me C(═O)tBu racemic VI-480 Me Me Me NH Ph CH₂ Me Me C(═O)tBu (S)- VI-481 Me Et Me NH Ph CH₂ H H C(═O)tBu racemic VI-482 Me Et Me NH Ph CH₂ H H C(═O)tBu (S)- VI-483 Me Et Me NH Ph CH₂ Me H C(═O)tBu racemic VI-484 Me Et Me NH Ph CH₂ Me H C(═O)tBu (S)- VI-485 Me Et Me NH Ph CH₂ H Me C(═O)tBu racemic VI-486 Me Et Me NH Ph CH₂ H Me C(═O)tBu (S)- VI-487 Me Et Me NH Ph CH₂ Me Me C(═O)tBu racemic VI-488 Me Et Me NH Ph CH₂ Me Me C(═O)tBu (S)- VI-489 Me Me Me NH Ph CH₂ H H C(═O)OEt racemic VI-490 Me Me Me NH Ph CH₂ H H C(═O)OEt (S)- VI-491 Me Me Me NH Ph CH₂ Me H C(═O)OEt racemic VI-492 Me Me Me NH Ph CH₂ Me H C(═O)OEt (S)- VI-493 Me Me Me NH Ph CH₂ H Me C(═O)OEt racemic VI-494 Me Me Me NH Ph CH₂ H Me C(═O)OEt (S)- VI-495 Me Me Me NH Ph CH₂ Me Me C(═O)OEt racemic VI-496 Me Me Me NH Ph CH₂ Me Me C(═O)OEt (S)- VI-497 Me Et Me NH Ph CH₂ H H C(═O)OEt racemic VI-498 Me Et Me NH Ph CH₂ H H C(═O)OEt (S)- VI-499 Me Et Me NH Ph CH₂ Me H C(═O)OEt racemic VI-500 Me Et Me NH Ph CH₂ Me H C(═O)OEt (S)- VI-501 Me Et Me NH Ph CH₂ H Me C(═O)OEt racemic VI-502 Me Et Me NH Ph CH₂ H Me C(═O)OEt (S)-

TABLE 161 (VIc)

Com- Con- pound figu- No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ ration VI-503 Me Et Me NH Ph CH₂ Me Me C(═O)OEt racemic VI-504 Me Et Me NH Ph CH₂ Me Me C(═O)OEt (S)- VI-505 Me Me Me NH Ph CH₂ H H C(═O)Oc racemic Hex VI-506 Me Me Me NH Ph CH₂ H H C(═O)Oc (S)- Hex VI-507 Me Me Me NH Ph CH₂ Me H C(═O)Oc racemic Hex VI-508 Me Me Me NH Ph CH₂ Me H C(═O)Oc S)- Hex VI-509 Me Me Me NH Ph CH₂ H Me C(═O)Oc racemic Hex VI-510 Me Me Me NH Ph CH₂ H Me C(═O)Oc (S)- Hex VI-511 Me Me Me NH Ph CH₂ Me Me C(═O)Oc racemic Hex VI-512 Me Me Me NH Ph CH₂ Me Me C(═O)Oc (S)- Hex VI-513 Me Et Me NH Ph CH₂ H H C(═O)Oc racemic Hex VI-514 Me Et Me NH Ph CH₂ H H C(═O)Oc (S)- Hex VI-515 Me Et Me NH Ph CH₂ Me H C(═O)Oc racemic Hex VI-516 Me Et Me NH Ph CH₂ Me H C(═O)Oc (S)- Hex VI-517 Me Et Me NH Ph CH₂ H Me C(═O)Oc racemic Hex VI-518 Me Et Me NH Ph CH₂ H Me C(═O)Oc (S)- Hex VI-519 Me Et Me NH Ph CH₂ Me Me C(═O)Oc racemic Hex VI-520 Me Et Me NH Ph CH₂ Me Me C(═O)Oc (S)- Hex VI-521 Me Me Me CH₂ Ph CH₂ H H Me racemic VI-522 Me Me Me CH₂ Ph CH₂ H H Me (S)- VI-523 Me Me Me CH₂ Ph CH₂ Me H Me racemic VI-524 Me Me Me CH₂ Ph CH₂ Me H Me (S)- VI-525 Me Me Me CH₂ Ph CH₂ H Me Me racemic VI-526 Me Me Me CH₂ Ph CH₂ H Me Me (S)- VI-527 Me Me Me CH₂ Ph CH₂ Me Me Me racemic VI-528 Me Me Me CH₂ Ph CH₂ Me Me Me (S)- VI-529 Me Et Me CH₂ Ph CH₂ H H Me racemic VI-530 Me Et Me CH₂ Ph CH₂ H H Me (S)- VI-531 Me Et Me CH₂ Ph CH₂ Me H Me racemic VI-532 Me Et Me CH₂ Ph CH₂ Me H Me (S)- VI-533 Me Et Me CH₂ Ph CH₂ H Me Me racemic VI-534 Me Et Me CH₂ Ph CH₂ H Me Me (S)- VI-535 Me Et Me CH₂ Ph CH₂ Me Me Me racemic VI-536 Me Et Me CH₂ Ph CH₂ Me Me Me (S)- VI-537 Me Me Me CH₂ Ph CH₂ H H Et racemic VI-538 Me Me Me CH₂ Ph CH₂ H H Et (S)- VI-539 Me Me Me CH₂ Ph CH₂ Me H Et racemic VI-540 Me Me Me CH₂ Ph CH₂ Me H Et (S)- VI-541 Me Me Me CH₂ Ph CH₂ H Me Et racemic VI-542 Me Me Me CH₂ Ph CH₂ H Me Et (S)- VI-543 Me Me Me CH₂ Ph CH₂ Me Me Et racemic VI-544 Me Me Me CH₂ Ph CH₂ Me Me Et (S)- VI-545 Me Et Me CH₂ Ph CH₂ H H Et racemic VI-546 Me Et Me CH₂ Ph CH₂ H H Et (S)- VI-547 Me Et Me CH₂ Ph CH₂ Me H Et racemic VI-548 Me Et Me CH₂ Ph CH₂ Me H Et (S)- VI-549 Me Et Me CH₂ Ph CH₂ H Me Et racemic VI-550 Me Et Me CH₂ Ph CH₂ H Me Et (S)- VI-551 Me Et Me CH₂ Ph CH₂ Me Me Et racemic VI-552 Me Et Me CH₂ Ph CH₂ Me Me Et (S)-

TABLE 162 (VIc)

Com- Con- pound figu- No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ ration VI-841 Me Me Me NH Ph (CH₂)₂ H H Me racemic VI-842 Me Me Me NH Ph (CH₂)₂ H H Me (R)- VI-843 Me Me Me NH Ph (CH₂)₂ Me H Me racemic VI-844 Me Me Me NH Ph (CH₂)₂ Me H Me (R)- VI-845 Me Me Me NH Ph (CH₂)₂ H Me Me racemic VI-846 Me Me Me NH Ph (CH₂)₂ H Me Me (R)- VI-847 Me Me Me NH Ph (CH₂)₂ Me Me Me racemic VI-848 Me Me Me NH Ph (CH₂)₂ Me Me Me (R)- VI-849 Me Et Me NH Ph (CH₂)₂ H H Me racemic VI-850 Me Et Me NH Ph (CH₂)₂ H H Me (R)- VI-851 Me Et Me NH Ph (CH₂)₂ Me H Me racemic VI-852 Me Et Me NH Ph (CH₂)₂ Me H Me (R)- VI-853 Me Et Me NH Ph (CH₂)₂ H Me Me racemic VI-854 Me Et Me NH Ph (CH₂)₂ H Me Me (R)- VI-855 Me Et Me NH Ph (CH₂)₂ Me Me Me racemic VI-856 Me Et Me NH Ph (CH₂)₂ Me Me Me (R)- VI-857 Me Me Me NH Ph (CH₂)₂ H H C(═O)Me racemic VI-858 Me Me Me NH Ph (CH₂)₂ H H C(═O)Me (R)- VI-859 Me Me Me NH Ph (CH₂)₂ Me H C(═O)Me racemic VI-860 Me Me Me NH Ph (CH₂)₂ Me H C(═O)Me (R)- VI-861 Me Me Me NH Ph (CH₂)₂ H Me C(═O)Me racemic VI-862 Me Me Me NH Ph (CH₂)₂ H Me C(═O)Me (R)- VI-863 Me Me Me NH Ph (CH₂)₂ Me Me C(═O)Me racemic VI-864 Me Me Me NH Ph (CH₂)₂ Me Me C(═O)Me (R)- VI-865 Me Et Me NH Ph (CH₂)₂ H H C(═O)Me racemic VI-866 Me Et Me NH Ph (CH₂)₂ H H C(═O)Me (R)- VI-867 Me Et Me NH Ph (CH₂)₂ Me H C(═O)Me racemic VI-868 Me Et Me NH Ph (CH₂)₂ Me H C(═O)Me (R)- VI-869 Me Et Me NH Ph (CH₂)₂ H Me C(═O)Me racemic VI-870 Me Et Me NH Ph (CH₂)₂ H Me C(═O)Me (R)- VI-871 Me Et Me NH Ph (CH₂)₂ Me Me C(═O)Me racemic VI-872 Me Et Me NH Ph (CH₂)₂ Me Me C(═O)Me (R)- VI-873 Me Me Me NH Ph (CH₂)₂ H H C(═O)Et racemic VI-874 Me Me Me NH Ph (CH₂)₂ H H C(═O)Et (R)- VI-875 Me Me Me NH Ph (CH₂)₂ Me H C(═O)Et racemic VI-876 Me Me Me NH Ph (CH₂)₂ Me H C(═O)Et (R)- VI-877 Me Me Me NH Ph (CH₂)₂ H Me C(═O)Et racemic VI-878 Me Me Me NH Ph (CH₂)₂ H Me C(═O)Et (R)- VI-879 Me Me Me NH Ph (CH₂)₂ Me Me C(═O)Et racemic VI-880 Me Me Me NH Ph (CH₂)₂ Me Me C(═O)Et (R)- VI-881 Me Et Me NH Ph (CH₂)₂ H H C(═O)Et racemic VI-882 Me Et Me NH Ph (CH₂)₂ H H C(═O)Et (R)- VI-883 Me Et Me NH Ph (CH₂)₂ Me H C(═O)Et racemic VI-884 Me Et Me NH Ph (CH₂)₂ Me H C(═O)Et (R)- VI-885 Me Et Me NH Ph (CH₂)₂ H Me C(═O)Et racemic VI-886 Me Et Me NH Ph (CH₂)₂ H Me C(═O)Et (R)- VI-887 Me Et Me NH Ph (CH₂)₂ Me Me C(═O)Et racemic VI-888 Me Et Me NH Ph (CH₂)₂ Me Me C(═O)Et (R)- VI-889 Me Me Me — Ph — H H Me racemic VI-890 Me Me Me — Ph — H H Me (R)-

TABLE 163 (VIc)

Com- pound Con- No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ figuration VI-891 Me Me Me — Ph — Me H Me racemic VI-892 Me Me Me — Ph — Me H Me (R)- VI-893 Me Me Me — Ph — H Me Me racemic VI-894 Me Me Me — Ph — H Me Me (R)- VI-895 Me Me Me — Ph — Me Me Me racemic VI-896 Me Me Me — Ph — Me Me Me (R)- VI-897 Me Et Me — Ph — H H Me racemic VI-898 Me Et Me — Ph — H H Me (R)- VI-899 Me Et Me — Ph — Me H Me racemic VI-900 Me Et Me — Ph — Me H Me (R)- VI-901 Me Et Me — Ph — H Me Me racemic VI-902 Me Et Me — Ph — H Me Me (R)- VI-903 Me Et Me — Ph — Me Me Me racemic VI-904 Me Et Me — Ph — Me Me Me (R)- VI-905 Me Me Me — Ph — H H C(═O)Me racemic VI-906 Me Me Me — Ph — H H C(═O)Me (R)- VI-907 Me Me Me — Ph — Me H C(═O)Me racemic VI-908 Me Me Me — Ph — Me H C(═O)Me (R)- VI-909 Me Me Me — Ph — H Me C(═O)Me racemic VI-910 Me Me Me — Ph — H Me C(═O)Me (R)- VI-911 Me Me Me — Ph — Me Me C(═O)Me racemic VI-912 Me Me Me — Ph — Me Me C(═O)Me (R)- VI-913 Me Et Me — Ph — H H C(═O)Me racemic VI-914 Me Et Me — Ph — H H C(═O)Me (R)- VI-915 Me Et Me — Ph — Me H C(═O)Me racemic VI-916 Me Et Me — Ph — Me H C(═O)Me (R)- VI-917 Me Et Me — Ph — H Me C(═O)Me racemic VI-918 Me Et Me — Ph — H Me C(═O)Me (R)- VI-919 Me Et Me — Ph — Me Me C(═O)Me racemic VI-920 Me Et Me — Ph — Me Me C(═O)Me (R)- VI-921 Me Me Me — Ph — H H C(═O)Et racemic VI-922 Me Me Me — Ph — H H C(═O)Et (R)- VI-923 Me Me Me — Ph — Me H C(═O)Et racemic VI-924 Me Me Me — Ph — Me H C(═O)Et (R)- VI-925 Me Me Me — Ph — H Me C(═O)Et racemic VI-926 Me Me Me — Ph — H Me C(═O)Et (R)- VI-927 Me Me Me — Ph — Me Me C(═O)Et racemic VI-928 Me Me Me — Ph — Me Me C(═O)Et (R)- VI-929 Me Et Me — Ph — H H C(═O)Et racemic VI-930 Me Et Me — Ph — H H C(═O)Et (R)- VI-931 Me Et Me — Ph — Me H C(═O)Et racemic VI-932 Me Et Me — Ph — Me H C(═O)Et (R)- VI-933 Me Et Me — Ph — H Me C(═O)Et racemic VI-934 Me Et Me — Ph — H Me C(═O)Et (R)- VI-935 Me Et Me — Ph — Me Me C(═O)Et racemic VI-936 Me Et Me — Ph — Me Me C(═O)Et (R)- VI-937 Me Me Me — Ph CH₂ H H Me racemic VI-938 Me Me Me — Ph CH₂ H H Me (S)- VI-939 Me Me Me — Ph CH₂ Me H Me racemic VI-940 Me Me Me — Ph CH₂ Me H Me (S)-

TABLE 164 (VIc)

Com- pound Con- No. R¹ R² R³ L² R⁴ L³ R⁸ R⁹ R⁷ figuration VI-941 Me Me Me — Ph CH₂ H Me Me racemic VI-942 Me Me Me — Ph CH₂ H Me Me (S)- VI-943 Me Me Me — Ph CH₂ Me Me Me racemic VI-944 Me Me Me — Ph CH₂ Me Me Me (S)- VI-945 Me Et Me — Ph CH₂ H H Me racemic VI-946 Me Et Me — Ph CH₂ H H Me (S)- VI-947 Me Et Me — Ph CH₂ Me H Me racemic VI-948 Me Et Me — Ph CH₂ Me H Me (S)- VI-949 Me Et Me — Ph CH₂ H Me Me racemic VI-950 Me Et Me — Ph CH₂ H Me Me (S)- VI-951 Me Et Me — Ph CH₂ Me Me Me racemic VI-952 Me Et Me — Ph CH₂ Me Me Me (S)- VI-953 Me Me Me — Ph CH₂ H H C(═O)Me racemic VI-954 Me Me Me — Ph CH₂ H H C(═O)Me (S)- VI-955 Me Me Me — Ph CH₂ Me H C(═O)Me racemic VI-956 Me Me Me — Ph CH₂ Me H C(═O)Me (S)- VI-957 Me Me Me — Ph CH₂ H Me C(═O)Me racemic VI-958 Me Me Me — Ph CH₂ H Me C(═O)Me (S)- VI-959 Me Me Me — Ph CH₂ Me Me C(═O)Me racemic VI-960 Me Me Me — Ph CH₂ Me Me C(═O)Me (S)- VI-961 Me Et Me — Ph CH₂ H H C(═O)Me racemic VI-962 Me Et Me — Ph CH₂ H H C(═O)Me (S)- VI-963 Me Et Me — Ph CH₂ Me H C(═O)Me racemic VI-964 Me Et Me — Ph CH₂ Me H C(═O)Me (S)- VI-965 Me Et Me — Ph CH₂ H Me C(═O)Me racemic VI-966 Me Et Me — Ph CH₂ H Me C(═O)Me (S)- VI-967 Me Et Me — Ph CH₂ Me Me C(═O)Me racemic VI-968 Me Et Me — Ph CH₂ Me Me C(═O)Me (S)- VI-969 Me Me Me — Ph CH₂ H H C(═O)Et racemic VI-970 Me Me Me — Ph CH₂ H H C(═O)Et (S)- VI-971 Me Me Me — Ph CH₂ Me H C(═O)Et racemic VI-972 Me Me Me — Ph CH₂ Me H C(═O)Et (S)- VI-973 Me Me Me — Ph CH₂ H Me C(═O)Et racemic VI-974 Me Me Me — Ph CH₂ H Me C(═O)Et (S)- VI-975 Me Me Me — Ph CH₂ Me Me C(═O)Et racemic VI-976 Me Me Me — Ph CH₂ Me Me C(═O)Et (S)- VI-977 Me Et Me — Ph CH₂ H H C(═O)Et racemic VI-978 Me Et Me — Ph CH₂ H H C(═O)Et (S)- VI-979 Me Et Me — Ph CH₂ Me H C(═O)Et racemic VI-980 Me Et Me — Ph CH₂ Me H C(═O)Et (S)- VI-981 Me Et Me — Ph CH₂ H Me C(═O)Et racemic VI-982 Me Et Me — Ph CH₂ H Me C(═O)Et (S)- VI-983 Me Et Me — Ph CH₂ Me Me C(═O)Et racemic VI-984 Me Et Me — Ph CH₂ Me Me C(═O)Et (S)-

Advantageous Effects of Invention

As for a novel substituted dihydropyrrolopyrazole compound having a particular structure represented by formula (I) of the present invention or a pharmacologically acceptable salt thereof, the compound itself or a metabolite thereof has excellent CDK7 inhibitory activity, high selectivity for a kinase inhibitory effect, and excellent safety. Thus, the compound represented by formula (I) or the pharmacologically acceptable salt thereof is pharmaceutically useful as a therapeutic agent and/or a prophylactic agent for cancers or inflammatory diseases.

DESCRIPTION OF EMBODIMENTS

One embodiment of the present invention will be described below. In the present specification, each “compound represented by formula (I)”, etc. is also referred to as “compound (I)”, etc. for the sake of convenience. Various substituents defined or illustrated below can be arbitrarily selected and combined.

In the present specification, the “prodrug” means a compound or a salt thereof which forms a compound having a CDK7 inhibitory effect by undergoing metabolic reaction when administered into an animal body.

One embodiment of the present invention is a compound represented by formula (I) or a pharmaceutically acceptable salt thereof.

In formula (I),

L¹ is an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

L² is a single bond, an oxygen atom, an optionally substituted nitrogen atom, an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

L³ is a single bond, an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenyl group, an optionally substituted linear or branched C₂₋₆ alkynyl group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group,

R¹, R², and R³ each independently are an optionally substituted linear or branched C₁₋₄ alkyl group, an optionally substituted linear or branched C₂₋₄ alkenyl group, an optionally substituted linear or branched C₂₋₄ alkynyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group,

R⁴ is a hydrogen atom, an optionally substituted linear or branched C₁₋₆ alkyl group, an optionally substituted linear or branched C₂₋₆ alkenyl group, an optionally substituted linear or branched C₂₋₆ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₃₋₆ cycloalkenyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group, and

R⁵ is a hydrogen atom, an optionally substituted linear or branched C₁₋₁₆ alkyl group, an optionally substituted linear or branched C₂₋₁₆ alkenyl group, an optionally substituted linear or branched C₂₋₁₆ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₃₋₆ cycloalkenyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group.

In the present specification, the term “optionally substituted” means that the group concerned may be unsubstituted or may be further substituted by a substituent.

The substituent means a monovalent group, and examples thereof include linear or branched C₁₋₆ alkyl groups, C₃₋₆ cycloalkyl groups, linear or branched C₂₋₆ alkenyl groups, C₃₋₆ cycloalkenyl groups, linear or branched C₂₋₆ alkynyl groups, C₁₋₆ alkoxy groups, halogen atoms, a hydroxy group, a cyano group, an oxo group (═O), an amino group, C₁₋₆ alkylamino groups, a nitro group, a carboxy group (—COOH), a carbamoyl group (—CONH₂), N-mono-C₁₋₆ alkylcarbamoyl groups, N,N-di-C₁₋₆ alkylcarbamoyl groups, C₁₋₆ alkanoyloxy groups (—OCOR; R is a C₁₋₆ alkyl group), C₆₋₁₀ aryl groups, heterocyclic groups, C₆₋₁₀ aryloxy groups, C₇₋₁₂ aralkyl groups, and C₇₋₁₂ aralkyloxy groups. The substituent may be further substituted by a halogen atom, a hydroxy group, an amino group, a cyano group, an oxo group (═O), a linear or branched C₁₋₆ alkyl group, or the like. In the case where the substituent is an amino group or a carboxy group, the form may be a salt thereof.

In the case where the group concerned has two or more substituents, two substituents may be bonded to each other to form a cyclic structure. Examples of the case where two substituents are bonded to each other to form a cyclic structure include a cyclopropyl group, a cyclobutyl group, and a methylenedioxy group. Specifically, in the case where a methylenedioxy group is bonded to a benzene ring, the substituent becomes a 1,3-benzodioxole group; in the case where the same carbon atom of a 1,2-ethylene group has two methyl groups which are bonded to each other, the group becomes a group represented by the following formula (M-1) or (M-2); and in the case where the same carbon atom of a 1,2-ethylene group has a methyl group and an ethyl group and 2-position of the ethyl group is bonded to the methyl group, the group becomes a group represented by the following formula (N-1) or (N-2).

The linear or branched C₁₋₆ alkyl group described in the present specification means a linear or branched alkyl group having 1 to 6 carbon atoms. Examples of the linear or branched C₁₋₆ alkyl group include C₁₋₆ alkyl groups such as a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a pentyl group, an isopentyl group, a neopentyl group, a tert-pentyl group, a 1-ethylpropyl group, a 1-methylbutyl group, a 2-methylbutyl group, a 1,2-dimethylpropyl group, a hexyl group, a 1-methylpentyl group, a 2-methylpentyl group, a 3-methylpentyl group, a 4-methylpentyl group, a 1-ethylbutyl group, a 2-ethylbutyl group, a 1,1-dimethylbutyl group, a 2,2-dimethylbutyl group, a 3,3-dimethylbutyl group, a 1,2-dimethylbutyl group, a 1,3-dimethylbutyl group, and a 2,3-dimethylbutyl group. The substituent is preferably a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, or a tert-butyl group.

Examples of a C₁₋₆ alkyl group substituted by a halogen atom include a chloromethyl group, a bromomethyl group, an iodomethyl group, a difluoromethyl group, a dichloromethyl group, a dibromomethyl group, a diiodomethyl group, a trifluoromethyl group, a trichloromethyl group, a 1-fluoroethyl group, a 2-fluoroethyl group, a 2-chloroethyl group, a 2-bromoethyl group, a 2,2-difluoroethyl group, a 2,2,2-trifluoroethyl group, a pentafluoroethyl group, a 2,2-dichloroethyl group, a 2,2,2-trichloroethyl group, a 1-fluoropropyl group, a 2-fluoropropyl group, a 3-fluoropropyl group, a 3,3,3-trifluoropropyl group, a perfluoropropyl group, a 1-fluoromethylethyl group, a 1-difluoromethylethyl group, a 1-trifluoromethylethyl group, a 1-fluoro-1-methylethyl group, a 4-fluorobutyl group, a perfluorobutyl group, a 5-fluoropentyl group, a perfluoropentyl group, a 6-fluorohexyl group, and a perfluorohexyl group.

A C₁₋₆ alkyl group substituted by an aryl group may be, for example, a C₇₋₁₁ aralkyl group. The C₇₋₁₁ aralkyl group means an alkyl group having an aryl group and having a total of 7 to 11 carbon atoms, and examples thereof include a benzyl group, a phenylethyl group, and a naphthylmethyl group.

The C₃₋₆ cycloalkyl group described in the present specification means a cyclic alkyl group having 3 to 6 carbon atoms. Examples of the C₃₋₆ cycloalkyl group include: monocyclic rings such as a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, and a cyclohexyl group; condensed rings such as a bicyclo[3.1.0]hexyl group; and spiro rings such as a spiro[2.3]hexyl group. The substituent is preferably a cyclopropyl group or a cyclobutyl group.

The linear or branched C₂₋₆ alkenyl group described in the present specification means a linear or branched alkenyl group having 2 to 6 carbon atoms. Examples of the linear or branched C₂₋₆ alkenyl group include alkenyl groups such as a vinyl group, a propen-1-yl group, a propen-2-yl group, a 1-butenyl group, a 2-butenyl group, a 3-butenyl group, a 1-methyl-1-propenyl group, a 2-methyl-1-propenyl group, a 1-pentenyl group, a 2-pentenyl group, a 3-pentenyl group, a 4-pentenyl group, a 5-pentenyl group, a 1-methyl-1-butenyl group, a 2-methyl-1-butenyl group, a 3-methyl-1-butenyl group, a 4-methyl-1-butenyl group, a 1-methyl-2-butenyl group, a 2-methyl-2-butenyl group, a 3-methyl-2-butenyl group, a 4-methyl-2-butenyl group, a 1-methyl-3-butenyl group, a 2-methyl-3-butenyl group, a 3-methyl-3-butenyl group, a 4-methyl-3-butenyl group, a 1,2-dimethyl-1-propenyl group, a 1-hexenyl group, a 2-hexenyl group, a 3-hexenyl group, a 4-hexenyl group, a 5-hexenyl group, a 6-hexenyl group, and structural isomers thereof.

The C₃₋₆ cycloalkenyl group described in the present specification means a cycloalkenyl group having 3 to 6 carbon atoms. Examples of the C₃₋₆ cycloalkenyl group include a cyclopropenyl group, a cyclobutenyl group, a cyclopentenyl group, and a cyclohexenyl group.

The C₂₋₆ alkynyl group described in the present specification means an alkynyl group having 2 to 6 carbon atoms. Examples of the C₂₋₆ alkynyl group include an ethynyl group, a propargyl group, a butynyl group, a pentynyl group, and a hexynyl group.

The C₁₋₆ alkoxy group described in the present specification means a group consisting of an oxy group (—O—) and a linear or branched C₁₋₆ alkyl group or a C₃₋₆ cycloalkyl group bonded to the oxy group. Examples of the C₁₋₆ alkoxy group include a methoxy group, an ethoxy group, a propyloxy group, an isopropyloxy group, a cyclopropyloxy group, a butoxy group, a cyclobutyloxy group, a pentyloxy group, a cyclopentyloxy group, a hexyloxy group, and a cyclohexyloxy group.

The C₁₋₆ alkylamino group described in the present specification means an amino group substituted by one or two independently selected aforementioned linear or branched C₁₋₆ alkyl groups or C₃₋₆ cycloalkyl groups. Examples of the C₁₋₆ alkylamino group include a methylamino group, an ethylamino group, a propylamino group, an isopropylamino group, a cyclopropylamino group, a butoxy group, a cyclobutylamino group, a pentylamino group, a cyclopentylamino group, a hexylamino group, a cyclohexylamino group, a dimethylamino group, a diethylamino group, an ethylmethylamino group, an isopropylmethylamino group, and a cyclopropylmethylamino group.

The halogen atom described in the present specification means a fluorine atom, a chlorine atom, a bromine atom, or an iodine atom.

The C₆₋₁₀ aryl group described in the present specification means an aryl group having 6 to 10 carbon atoms. Examples of the C₆₋₁₀ aryl group include a phenyl group and a naphthyl group.

The heterocyclic group described in the present specification means a cyclic group having at least one nitrogen atom, oxygen atom, or sulfur atom and may be an aromatic heterocyclic group or may be a nonaromatic heterocyclic group. Examples of the aromatic heterocyclic group include a pyridine group, a pyrimidine group, a pyridazine group, a pyrazine group, a triazine group, a pyrrole group, an imidazole group, a pyrazole group, an indole group, an indazole group, a furan group, a benzofuran group, a thiophene group, a benzothiophene group, a thiazole group, an isothiazole group, an oxazole group, an isoxazole group, and an oxadiazole group. Examples of the nonaromatic heterocyclic group include a pyrrolidinyl group, a piperidinyl group, a piperazinyl group, a morpholinyl group, and a thiomorpholinyl group.

The C₆₋₁₀ aryloxy group described in the present specification means a group consisting of an oxy group (—O—) and the aforementioned C₆₋₁₀ aryl group bonded to the oxy group. Examples of the C₆₋₁₀ aryloxy group include a phenyloxy group, a 1-naphthyloxy group, and a 2-naphthyloxy group.

The C₇₋₁₂ aralkyl group described in the present specification means the aforementioned C₁₋₆ alkyl group substituted by the aforementioned C₆₋₁₀ aryl group. Examples of the C₇₋₁₂ aralkyl group include a benzyl group, a phenylethyl group, a naphthylmethyl group, and a naphthylethyl group.

The C₇₋₁₂ aralkyloxy group described in the present specification means a group consisting of an oxy group (—O—) and the aforementioned C₇₋₁₂ aralkyl group bonded to the oxy group. Examples of the C₇₋₁₂ aralkyloxy group include a benzyloxy group, a phenylethyloxy group, a naphthylmethyloxy group, and a naphthylethyloxy group.

The linear or branched C₁₋₆ alkylene group as L¹, L², or L³ means a divalent group prepared by further removing one hydrogen atom from the aforementioned C₁₋₆ alkyl group. Examples of the C₁₋₆ alkylene group include a methylene group, a 1,1-ethylene group, a 1,2-ethylene group, a 1,1-propylene group, a 1,2-propylene group, a 2,2-propylene group, and a 1,3-propylene group.

The linear or branched C₂₋₆ alkenylene group as L¹, L², or L³ means a divalent group prepared by further removing one hydrogen atom from the aforementioned C₂₋₆ alkenyl group. Examples of the C₂₋₆ alkenylene group include a vinylene group and a propenylene group.

The linear or branched C₂₋₆ alkynylene group as L¹, L², or L³ means a divalent group prepared by further removing one hydrogen atom from the aforementioned C₂₋₆ alkynyl group. Examples of the C₂₋₆ alkynylene group include an ethynylene group and a propynylene group.

The C₃₋₆ cycloalkylene group as L¹, L², or L³ means a divalent group prepared by further removing one hydrogen atom from the aforementioned C₃₋₆ cycloalkyl group, and examples thereof include a 1,1-cyclopropylene group, a 1,2-cyclopropylene group, a 1,1-cyclobutylene group, a 1,2-cyclobutylene group, a 1,3-cyclobutylene group, a 1,4-cyclobutylene group, a 1,1-cyclopentylene group, a 1,2-cyclopentylene group, a 1,3-cyclopentylene group, a 1,1-cyclohexylene group, a 1,2-cyclohexylene group, a 1,3-cyclohexylene group, a 1,4-cyclohexylene group, a 5,5-spiro[2.3]hexylene group, and a 6,6-bicyclo[3.1.0]hexylene group.

The C₃₋₆ cycloalkenylene group as L¹, L², or L³ means a divalent group prepared by further removing one hydrogen atom from the aforementioned C₃₋₆ cycloalkenyl group, and examples thereof include a 1,2-cyclopropenylene group, a 1,2-cyclobutenylene group, a 1,3-cyclobutenylene group, a 3,3-cyclobutenylene group, a 1,2-cyclopentenylene group, a 1,2-cyclopentenylene group, a 1,3-cyclopentenylene group, a 3,3-cyclopentenylene group, a 4,4-cyclopentenylene group, a 1,2-cyclohexenylene group, a 1,3-cyclohexenylene group, a 1,3-cyclohexenylene group, a 1,3-cyclohexenylene group, a 3,3-cyclohexenylene group, and a 4,4-cyclohexenylene group.

The optionally substituted nitrogen atom as L² may be an unsubstituted nitrogen atom (divalent amino group represented by —NH—) or may be a divalent amino group having the aforementioned substituent bonded to the nitrogen atom.

The linear or branched C₁₋₄ alkyl group as R¹, R², or R³ is a linear or branched alkyl group having 1 to 4 carbon atoms and corresponds to one having 1 to 4 carbon atoms among the C₁₋₆ alkyl groups described above.

The linear or branched C₂₋₄ alkenyl group as R¹, R², or R³ is a linear or branched alkenyl group having 2 to 4 carbon atoms and corresponds to one having 2 to 4 carbon atoms among the C₂₋₆ alkenyl groups described above.

The linear or branched C₂₋₄ alkynyl group as R¹, R², or R³ is a linear or branched alkynyl group having 2 to 4 carbon atoms and corresponds to one having 2 to 4 carbon atoms among the C₂₋₆ alkynyl groups described above.

The linear or branched C₁₋₆ alkyl group, the linear or branched C₂₋₆ alkenyl group, the linear or branched C₂₋₆ alkynyl group, the C₆₋₁₀ aryl group, and the heterocyclic group as R⁴ are defined as in the substituents described above.

The linear or branched C₁₋₁₆ alkyl group as R⁵ means an alkyl group having 1 to 16 carbon atoms. Examples of the linear or branched C₁₋₁₆ alkyl group include C₁₋₁₆ alkyl groups such as a methyl group, an ethyl group, a propyl group, a butyl group, an isobutyl group, a pentyl group, an isopentyl group, a neopentyl group, a hexyl group, a heptyl group, an octyl group, a nonyl group, a decyl group, an undecyl group, a dodecyl group, a tridecyl group, a tetradecyl group, a pentadecyl group, and a hexadecyl group.

The linear or branched C₂₋₁₆ alkenyl group as R⁵ means a monovalent linear or branched alkenyl group having 2 to 16 carbon atoms, and the linear or branched C₂₋₁₆ alkynyl group means a monovalent linear or branched alkynyl group having 2 to 16 carbon atoms. The C₃₋₆ cycloalkyl group, the C₃₋₆ cycloalkenyl group, the C₆₋₁₀ aryl group, and the heterocyclic group as R⁵ are defined as in the substituents described above and L¹, etc.

The compound according to the present embodiment may be a compound represented by any chemical formula of formula (II), formula (III), or formula (IV).

In formula (II), formula (III), and formula (IV), L², L³, R¹, R², R³, R⁴, and R⁵ are defined as in formula (I).

In the formulas (I) to (IV), L² may be an oxygen atom, an unsubstituted nitrogen atom, or a methylene group. L³ may be a single bond, or an optionally substituted linear or branched C₁₋₆ alkylene group or C₂₋₆ alkynylene group, or may be a linear or branched C₁₋₆ alkylene group, C₂₋₆ alkenylene group, or C₂₋₆ alkynylene group substituted by an oxo group which forms an ester group together with the oxygen atom bonded to R⁵.

In the formulas (I) to (IV), R¹, R², and R³ may each independently be an optionally substituted linear or branched C₁₋₄ alkyl group. R⁴ may be a hydrogen atom, an optionally substituted linear or branched C₁₋₆ alkyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group. R⁵ may be a hydrogen atom, an optionally substituted linear or branched C₁₋₁₆ alkyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group.

In the formulas (I) to (IV), preferably, L² is a single bond or an unsubstituted nitrogen atom, L³ is a single bond or an optionally substituted linear or branched C₁₋₆ alkylene group, R¹, R², and R³ are each independently an optionally substituted linear or branched C₁₋₄ alkyl group, R⁴ is an optionally substituted linear or branched C₁₋₆ alkyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group, and R⁵ is a hydrogen atom, an optionally substituted linear or branched C₁₋₁₆ alkyl group, or an optionally substituted C₃₋₆ cycloalkyl group.

In the formulas (I) to (IV), more preferably, L² is a single bond or an unsubstituted nitrogen atom, L³ is a single bond or an optionally substituted linear or branched C₁₋₆ alkylene group, R¹, R², and R³ are each independently a linear or branched C₁₋₄ alkyl group, R⁴ is an optionally substituted linear or branched C₁₋₆ alkyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group, and R⁵ is a hydrogen atom, a linear or branched C₁₋₁₆ alkyl group, a linear or branched C₁₋₁₆ alkyl group substituted by a halogen atom, an oxo group, or a linear or branched C₁₋₆ alkyl group, or a C₃₋₆ cycloalkyl group optionally substituted by a halogen atom.

In the formulas (I) to (IV), particularly preferably, L² is a single bond or an unsubstituted nitrogen atom, L³ is a single bond or a group represented by the following formula (O-1), (O-2), (O-3), or (O-4), R¹, R², and R³ are each independently a linear or branched C₁₋₄ alkyl group, R⁴ is an optionally substituted phenyl group or thienyl group, and R⁵ is a hydrogen atom, a linear or branched C₁₋₁₆ alkyl group, a linear or branched C₁₋₁₆ alkyl group substituted by a halogen atom, or a C₃₋₆ cycloalkyl group. In the present specification, the chemical formula represented by formula (O-1) is also referred to as “C(Me)₂CH₂”, the chemical formula represented by formula (O-2) is also referred to as “CH₂C(Me)₂”, the chemical formula represented by formula (M-2) is also referred to as “CH₂-1,1-cyclopropylene”, and the chemical formula represented by formula (N-1) is also referred to as “1,1-cyclobutylene-CH₂”.

Among compounds (I) according to the present embodiment or pharmacologically acceptable salts thereof, a compound as represented by formula (V) wherein R⁵ is substituted by an oxo group, and the oxo group and the oxygen atom bonded to R⁵ form an ester bond, or a compound as represented by formula (VI) wherein R⁵ is an alkylene group substituted by a substituent containing an oxygen atom, and an acetal group containing the oxygen atom and the oxygen atom bonded to R⁵ is formed can be a compound that acts as a prodrug. The compound (V) or the compound (VI) tends to have better oral absorbability and skin penetration and can form compound (I) (wherein R⁵ is a hydrogen atom) by metabolism.

In formula (V) and formula (VI), R¹, R², R³, R⁴, L¹, L², and L³ are defined as in formula (I). R⁶ is a hydrogen atom, an optionally substituted linear or branched C₁₋₁₅ alkyl group, an optionally substituted linear or branched C₂₋₁₅ alkenyl group, an optionally substituted linear or branched C₂₋₁₅ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, an optionally substituted C₃₋₆ cycloalkenyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group, and R⁸ and R⁹ are each independently a hydrogen atom or a C₁₋₄ alkyl group. R⁷ is a linear or branched C₁₋₁₅ alkyl group optionally having a substituent, an optionally substituted linear or branched C₂₋₁₅ alkenyl group, an optionally substituted linear or branched C₂₋₁₅ alkynyl group, an optionally substituted C₃₋₆ cycloalkyl group, or an optionally substituted C₃₋₆ cycloalkenyl group. The linear or branched C₁₋₁₅ alkyl group, the linear or branched C₂₋₁₅ alkenyl group, the linear or branched C₂₋₁₅ alkynyl group, the C₃₋₆ cycloalkyl group, the C₃₋₆ cycloalkenyl group, the C₆₋₁₀ aryl group, and the heterocyclic group as R⁶ or R⁷, and substituents added to these are defined as in the groups in the formulas (I) to (IV).

R⁶ may be an optionally substituted linear or branched C₁₋₁₅ alkyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted C₁₋₁₅ alkoxy group. R⁷ may be an optionally substituted linear or branched C₁₋₁₆ alkyl group.

In formula (V), preferably, L¹ is a cyclopropylene group or a cyclobutylene group, L² is a single bond or an unsubstituted nitrogen atom, L³ is a single bond or an optionally substituted linear or branched C₁₋₆ alkylene group, R¹, R², and R³ are each independently an optionally substituted linear or branched C₁₋₄ alkyl group, R⁴ is an optionally substituted linear or branched C₁₋₆ alkyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group, and R⁶ is an optionally substituted linear or branched C₁₋₁₅ alkyl group.

In formula (V), more preferably, L¹ is a cyclobutylene group, L² is a single bond or an unsubstituted nitrogen atom, L³ is a single bond or an optionally substituted linear or branched C₁₋₆ alkylene group, R¹, R², and R³ are each independently a linear or branched C₁₋₄ alkyl group, R⁴ is an optionally substituted linear or branched C₁₋₆ alkyl group, an optionally substituted C₆₋₁₀ aryl group, or an optionally substituted heterocyclic group, and R⁶ is an optionally substituted linear or branched C₁₋₁₅ alkyl group.

The compound according to the present embodiment or a pharmacologically acceptable salt thereof is specifically a compound selected from a compound group shown below or a pharmacologically acceptable salt thereof.

-   (S)—N-(2-hydroxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-hydroxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-hydroxy-1-phenylethyl)-6,6-dimethyl-3-[2-methyl-2-(trimethylsilyl)propaneamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)-3-[1-(ethyldimethylsilyl)cyclobutanecarboxamido]-N-(2-hydroxy-1-phenylethyl)-6,6-dimethyl-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)-3-[2-(ethyldimethylsilyl)-2-methylpropaneamido]-N-(2-hydroxy-1-phenylethyl)-6,6-dimethyl-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-hydroxy-1-phenylethyl)-N,6,6-trimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5     (1H)-carboxamide, -   (S)-2-[(2-methoxypropan-2-yl)oxy]-1-phenylethyl6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate, -   (S)-2-hydroxy-1-phenylethyl -   6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate, -   2-Methoxy-1-phenylethyl -   6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate, -   N-[5-(4-hydroxy-3-phenylbutanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[5-(3-hydroxy-3-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)—N-(3-hydroxy-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5     (1H)-carboxamide, -   (R)—N-(3-hydroxy-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5     (1H)-carboxamide, -   (R)—N-(4-hydroxy-1-phenylbutyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5     (1H)-carboxamide, -   (R)—N-(5-hydroxy-1-phenylpentyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-hydroxy-2-methyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-hydroxy-2-methyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(3-hydroxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(3-hydroxy-3-methyl-1-phenylbutyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-methoxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-[2-(difluoromethoxy)-1-phenylethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-ethoxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(3-methoxy-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   Sodium -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylacetate, -   (R)—N-(2-hydroxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[1-(2-fluorophenyl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-[1-(3-fluorophenyl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-[1-(4-fluorophenyl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[2-hydroxy-1-(pyridin-2-yl)ethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[2-hydroxy-1-(pyridin-3-yl)ethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[1-(benzo[d][1,3]dioxol-4-yl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(1-cyclohexyl-2-hydroxyethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)     cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(1-hydroxy-3-methylbutan-2-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(1-hydroxypropan-2-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(2-hydroxyethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(2-hydroxy-2-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(2-hydroxypropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[(2S)-1-hydroxy-3-methyl-1-phenylbutan-2-yl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(4-hydroxy-1-phenyl-2-butyn-1-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     acetate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     propionate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     butanoate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     pentanoate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     octanoate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     dodecanoate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     palmitate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     isobutanoate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     pivalate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     3-methylbutanoate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     benzoate, -   (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl     ethylcarbonate, -   Sodium -   (S)-4-(2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethoxy)-4-oxobutanoate, -   (S)-(2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethoxy) -   methyl pivalate, -   (S)-2-acetoxy-1-phenylethyl -   6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate, -   (S)-benzyl -   2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylacetate, -   (S)-methyl -   2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylacetate, -   N-(2,2-difluoro-3-hydroxy-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(2-isopropoxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   6,6-Dimethyl-N-(2-phenoxy-1-phenylethyl)-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-[1-(2-chlorophenyl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-[2-hydroxy-1-(o-tolyl)ethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(1-hydroxy-3-phenylpropan-2-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(2-hydroxy-3-methylbutyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(1-hydroxy-3-phenylpropan-2-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(2-hydroxy-2-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (S)—N-(2-hydroxy-2-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   2-Hydroxy-2-phenylethyl -   6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate, -   (R)—N-[6,6-dimethyl-5-(2-phenoxypropanoyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (S)—N-[6,6-dimethyl-5-(2-phenoxypropanoyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[6,6-dimethyl-5-(2-phenoxyacetyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)—N-[6,6-dimethyl-5-(2-phenoxypropanoyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclopropanecarboxamide, -   N-{5-[3-(benzyloxy)-2-phenoxypropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[5-(3-hydroxy-2-phenoxypropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[2-(4-chlorophenoxy)propanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[2-(2-chlorophenoxy)propanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[2-(cyclohexyloxy)propanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[2-(3-chlorophenoxy)propanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[5-(2-methoxypropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[5-(3-methoxy-2-phenoxypropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydro     pyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{6,6-dimethyl-5-[2-(pyridin-3-yloxy)propanoyl]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[3-(dimethylamino)-2-phenoxypropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[6,6-dimethyl-5-(2-phenoxy-2-phenylacetyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[3-(3,3-difluoropyrrolidin-1-yl)-2-phenoxypropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[5-(3-hydroxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (S)—N-[5-(3-hydroxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide -   (R)—N-{5-[3-(benzyloxy)-2-phenylpropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)—N-[5-(3-hydroxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide -   (R)—N-[5-(2-methoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (S)—N-[5-(2-methoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[5-(3-methoxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-[5-(4-methoxy-2-phenylbutanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (S)—N-[5-(3-hydroxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclopropanecarboxamide, -   (R)—N-[5-(2-methoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclopropanecarboxamide, -   (R)—N-{5-[2-(difluoromethoxy)-2-phenylacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)—N-[5-(2-ethoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)-1-(ethyldimethylsilyl)-N-[5-(2-methoxy-2-phenylacetyl)-6,6-dimeth     yl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]cyclobutanecarboxamide, -   (R)—N-[5-(2-cyclopropoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)—N-[5-(2-isopropoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)—N-{6,6-dimethyl-5-[2-phenyl-2-(trifluoromethoxy)acetyl]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)—N-[6,6-dimethyl-5-(2-phenyl-2-propoxyacetyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[2-(4-fluorophenyl)-2-methoxyacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[2-(3-fluorophenyl)-2-methoxyacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   (R)—N-{5-[2-(2-fluorophenyl)-2-methoxyacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{5-[2-methoxy-2-(thiophen-2-yl)acetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   (−)-N-{5-[2-methoxy-2-(thiophen-2-yl)acetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   (+)-N-{5-[2-methoxy-2-(thiophen-2-yl)acetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide, -   N-{[1-(hydroxymethyl)cyclobutyl](phenyl)methyl}-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-[2-(1-hydroxycyclopropyl)-1-phenylethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(3-ethyl-3-hydroxy-1-phenylpentyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-[1-(4-fluorophenyl)-3-hydroxy-3-methylbutyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-[1-(3-fluorophenyl)-3-hydroxy-3-methylbutyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-[1-(2-fluorophenyl)-3-hydroxy-3-methylbutyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(5-hydroxy-2,5-dimethylhexan-3-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[1-(4-fluorophenyl)-3-hydroxy2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[1-(3-fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (−)-N-[1-(3-fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (+)-N-[1-(3-fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-[1-(2-fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(1-hydroxy-2,2,4-trimethylpentan-3-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-(3-hydroxy-3-methyl-1-phenylbutyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   N-(3-hydroxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (−)-N-(3-hydroxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (+)-N-(3-hydroxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide, -   (R)—N-[5-(2-butoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide,     and -   N-(3-methoxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide.

The compound or the pharmacologically acceptable salt thereof according to the present embodiment may be a single optically active form or may be a mixture of a plurality of optically active forms.

In the case where geometric isomers or rotational isomers are present in the compound according to the present embodiment, these isomers are also included in the scope of the present invention, and in the case where proton tautomers are present, these tautomers are also encompassed in the present invention.

The “pharmacologically acceptable salt” according to the present embodiment is not particularly limited as long as being a salt acceptable as a drug, and examples thereof include: salts with inorganic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, nitric acid, sulfuric acid, and phosphoric acid; salts with organic carboxylic acids such as acetic acid, fumaric acid, maleic acid, succinic acid, citric acid, tartaric acid, adipic acid, lactic acid, and trifluoroacetic acid; salts with organic sulfonic acids such as methanesulfonic acid, trifluoromethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, and naphthalenesulfonic acid; salts with alkali metals such as lithium, sodium, and potassium; salts with alkaline earth metals such as calcium and magnesium; and quaternary ammonium salts such as ammonia, morpholine, glucosamine, ethylenediamine, guanidine, diethylamine, triethylamine, dicyclohexylamine, diethanolamine, and piperazine.

The compound or the pharmacologically acceptable salt thereof according to the present embodiment can form a hydrate or a solvate, and each one or a mixture thereof is encompassed in the present invention.

The compound according to the present embodiment may contain a non-natural ratio of an atomic isotope for one or more of the constituting atoms. Examples of the atomic isotope include deuterium (²H), tritium (³H), carbon-14 (¹⁴C), fluorine-18 (¹⁸F), sulfur-35 (³⁵S), and iodine-125 (¹²⁵I). These compounds are useful as therapeutic or prophylactic agents, research reagents, for example, assay reagents, and diagnostic agents, for example, in vivo diagnostic imaging agents. All isotopic variants of the compound according to the present embodiment are encompassed in the present invention, regardless of whether to be radioactive.

The compound or the pharmacologically acceptable salt thereof according to the present embodiment can be used as a pharmaceutical composition, if necessary, by adding an excipient, a lubricant, a binder, a disintegrant, a coating agent, a stabilizer, a tonicity agent, a buffer, a pH adjuster, a solubilizer, a thickener, a preservative, an antioxidant, a sweetener, a colorant, a flavor, and the like. The pharmaceutical composition can be appropriately prepared according to a purpose by a known method described in, for example, General Rules for Preparations, Japanese Pharmacopoeia 16th edition.

In the pharmaceutical composition, the content of the compound or the pharmacologically acceptable salt thereof according to the present embodiment can be appropriately adjusted.

The pharmaceutical composition can be in a dosage form described in General Rules for Preparations, Japanese Pharmacopoeia 16th edition, for example, a preparation for oral administration such as tablets, capsules, granules, or powders, or a preparation for parenteral administration such as injections (e.g., intravenous administration, subcutaneous administration, intramuscular administration, and intraperitoneal administration), eye drops, nasal drops, suppositories, ointments, lotions, creams, gels, sprays, patches, inhalants, or percutaneous absorption preparations.

Examples of the excipient include lactose, mannitol, starch, crystalline cellulose, light anhydrous silicic acid, calcium carbonate, and calcium hydrogen phosphate, and examples of the lubricant include stearic acid, magnesium stearate, and talc. Examples of the binder include starch, hydroxypropylcellulose, hydroxypropylmethylcellulose, and polyvinylpyrrolidone, and examples of the disintegrant include carboxymethylcellulose, low-substituted hydroxypropylmethylcellulose, and calcium citrate. Examples of the coating agent include hydroxypropylmethylcellulose, macrogol, and silicone resins, and examples of the stabilizer include ethyl p-hydroxybenzoate and benzyl alcohol.

Examples of the tonicity agent include glycerin, propylene glycol, sodium chloride, potassium chloride, sorbitol, and mannitol, examples of the buffer include boric acid, boric acid salts, phosphoric acid, phosphoric acid salts, citric acid, citric acid salts, acetic acid, acetic acid salts, ε-aminocaproic acid, and trometamol, and examples of the pH adjuster include hydrochloric acid, citric acid, phosphoric acid, glacial acetic acid, sodium hydroxide, potassium hydroxide, sodium carbonate, and sodium bicarbonate. Examples of the solubilizer include polysorbate 80, polyoxyethylene hydrogenated castor oil 60, macrogol 4000, purified soybean lecithin, and polyoxyethylene (160) polyoxypropylene (30) glycol, and examples of the thickener include cellulose polymers such as hydroxypropylmethylcellulose and hydroxypropylcellulose, polyvinyl alcohol, and polyvinylpyrrolidone. Examples of the stabilizer include edetic acid and sodium edetate, and examples of the preservative include sorbic acid, potassium sorbate, benzalkonium chloride, benzethonium chloride, methyl p-hydroxybenzoate, propyl p-hydroxybenzoate, and chlorobutanol.

Examples of ingredients that may be contained in pharmaceutical compositions for percutaneous administration such as ointments, lotions, creams, gels, patches, and sprays include: absorption promoters such as lauryl alcohol, myristyl alcohol, salicylic acid ethylene glycol, and pyrrothiodecane; fatty acid esters such as diisopropyl adipate, isopropyl myristate, cetyl lactate, myristyl lactate, isopropyl palmitate, diethyl sebacate, hexyl laurate, and cetyl isooctanoate; aliphatic alcohols such as cetyl alcohol, stearyl alcohol, oleyl alcohol, hexadecyl alcohol, and behenyl alcohol; glycols such as propylene glycol, propylenediol, polyethylene glycol, and dipropylene glycol; and surfactants such as sorbitan fatty acid ester, glycerin fatty acid ester, polyoxyethylene sorbitan fatty acid ester, polyoxyethylene glycerin fatty acid ester, polyethylene glycol fatty acid ester, polyoxyethylene alkyl ether, polyoxyethylene castor oil, and polyoxyethylene hydrogenated castor oil.

The dose of the compound or the pharmacologically acceptable salt thereof according to the present embodiment can be appropriately varied according to symptoms, age, a dosage form, etc. In the case of, for example, oral administration, it can usually be administered in one portion or several divided portions of 0.01 to 2000 mg, preferably 1 to 500 mg per day.

As for ointments, lotions, creams, or gels, one having a concentration of 0.00001% (w/v) to 10% (w/v), preferably 0.001% (w/v) to 5% (w/v) can usually be administered in one portion or several divided portions.

Next, a method for producing the compound or the pharmacologically acceptable salt thereof according to the present embodiment will be described. The compound or the pharmacologically acceptable salt thereof according to the present invention is not limited to compounds or pharmacologically acceptable salts thereof produced by production methods described below.

In the production methods given below, in the case where partial structures that inhibit the desired reactions or receive side reactions (e.g., a hydroxy group, an amino group, a carbonyl group, a carboxyl group, an amide group, a thiol group and the like) are present in compounds, the compounds of interest can be obtained by introducing protective groups to these partial structures, performing the desired reactions, and then removing the protective groups.

The introduction reaction and removal reaction of a protective group can be carried out according to a method routinely used in organic synthetic chemistry (e.g., a method described in, for example, Protective Groups in Organic Synthesis, 4th ed., T. W. Greene, P. G. M. Wuts, John Wiley & Sons Inc. (2006)).

Specific methods for producing the individual compounds of the present invention will be described in detail in Examples mentioned later.

Compound (I) can be produced, for example, by methods of production methods 1 to 4 given below with compound (A) as a starting material. A method for producing the compound (A) will be mentioned later.

<Production Method 1 for Compound (I)>

Production method 1 is a method for producing compound (I) through steps 1 to 3 with compound (A) as a starting material. Production method 1 is a suitable production method in the case where L² is an oxygen atom or an optionally substituted nitrogen atom. In production method 1, R¹, R², R³, R⁴, R⁵, L¹, L², and L³ are defined as in formula (I). P¹ group is a protective group for the amino group, and X is a leaving group. The P¹ group can substitute an acidic proton of pyrazole in the 4,6-dihydropyrrolo[3,4-c]pyrazole skeleton. Thus, the P¹ group may be added to position 1 of the 4,6-dihydropyrrolo[3,4-c]pyrazole skeleton or may be added to 2-position. Compound (A) will be described by using a chemical formula wherein it is added to 1-position of the 4,6-dihydropyrrolo[3,4-c]pyrazole skeleton, for the sake of convenience.

The P¹ group is not particularly limited as long as being a substituent known as a protective group for the amino group to those skilled in the art. Examples of the P¹ group include: optionally substituted C₇₋₁₁ aralkyl groups such as a benzyl group, a p-methoxyphenylmethyl group, and a o-nitrophenylmethyl group; optionally substituted acyl groups such as an acetyl group, a trifluoroacetyl group, and a benzoyl group; optionally substituted C₁₋₆ alkoxycarbonyl groups such as a methoxycarbonyl group, an ethoxycarbonyl group, a Boc group (tert-butoxycarbonyl group), a Cbz group (benzyloxycarbonyl group), a Fmoc group (fluorenylmethyloxycarbonyl group), and a Teoc group (trimethylsilylethyloxycarbonyl group); alkenyloxycarbonyl groups such as an Alloc group (allyloxycarbonyl group); alkylsulfonyl groups such as a methanesulfonyl group; and C₆₋₁₀ arylsulfonyl groups such as a p-toluenesulfonyl group.

The X group is not particularly limited as long as being a substituent known as a leaving group to those skilled in the art. Examples of X include: halogen atoms; an imidazolyl group; aminooxy groups such as a succinyl-N-oxy group and a benzotriazolyl-N-oxy group; and acyloxy groups such as a pivaloyloxy group and a benzoyloxy group. Alternatively, X may be a hydroxy group.

(Step 1)

Step 1 is the step of reacting compound (A) with an acylating agent to obtain compound (B).

As the acylating agent, for example, phosgene, diphosgene, triphosgene, carbonyldiimidazole (CDI), N,N′-disuccinimidyl carbonate, or carbonic acid ester can be used.

The amount of the acylating agent used is preferably 0.4 to 3.0 mol, more preferably 0.7 to 1.5 mol, with respect to 1 mol of the compound (A).

The reaction of step 1 may be performed in a solvent or may be performed without a solvent. In the case of using a solvent, there is no limitation as long as the solvent does not have influence on the reaction, and an organic solvent is preferred. Examples of the organic solvent include dichloromethane, 1,2-dichloroethane, diethyl ether, 1,2-dimethoxyethane, tetrahydrofuran (THF), N,N-dimethylformamide (DMF), and dimethyl sulfoxide (DMSO).

In step 1, a base can be further added in order to accelerate the reaction. Examples of the base include organic amines such as triethylamine, diisopropylethylamine (DIPEA), 1,5-diazabicyclo[4.3.0]nonene (DBN), 1,8-diazabicyclo[5.4.0]undecene (DBU), pyridine, and 4-dimethylaminopyridine (DMAP).

The amount of the base added is preferably 1 to 10 mol, more preferably 3 to 6 mol, with respect to 1 mol of the compound (A).

The reaction temperature of step 1 can be appropriately set by those skilled in the art. The reaction temperature is usually −100 to −20° C., preferably −80 to −60° C.

(Step 2)

Step 2 is the step of reacting compound (B) with compound (C) to obtain compound (D).

In step 2, the L² group is an oxygen atom or an optionally substituted nitrogen atom. Specifically, the compound (C) is an alcohol or an amine.

The amount of the compound (C) used is preferably 1 to 20 mol, more preferably 2 to 5 mol, with respect to 1 mol of the compound (B). The compound (C) and the compound (B) may be dissolved in an organic solvent and added to the reaction solution.

The reaction of step 2 may be performed in a solvent or may be performed without a solvent. In the case of using a solvent, there is no limitation as long as the solvent does not have influence on the reaction, and an organic solvent is preferred. Examples of the organic solvent include dichloromethane, 1,2-dichloroethane, diethyl ether, 1,2-dimethoxyethane, tetrahydrofuran (THF), 1,4-dioxane, N,N-dimethylformamide (DMF), and dimethyl sulfoxide (DMSO).

In step 2, a base can be further added in order to accelerate the reaction. Examples of the base include: organic amines such as triethylamine, diisopropylethylamine (DIPEA), 1,5-diazabicyclo[4.3.0]nonene (DBN), 1,8-diazabicyclo[5.4.0]undecene (DBU), pyridine, and 4-dimethylaminopyridine (DMAP); and inorganic bases such as potassium carbonate and sodium carbonate.

The amount of the base added is preferably 1 to 20 mol, more preferably 2 to 5 mol, with respect to 1 mol of the compound (A).

The reaction temperature of step 2 can be appropriately set by those skilled in the art. The reaction temperature is usually 0 to 120° C., preferably 25 to 100° C.

(Step 3)

Step 3 is the step of removing the P¹ group of compound (D) to produce compound (I).

The reaction conditions of step 3 can be appropriately selected by those skilled in the art according to the type of the P¹ group used. In the case where the P¹ group is, for example, an aralkyl group, it may be performed by hydrogenolysis or may be performed by using protonic acid or Lewis acid. In the case where the P¹ group is a Boc group, it can be performed by treatment with protonic acid or Lewis acid; in the case where the P¹ group is a Cbz group, it can be performed by hydrogenolysis or treatment with a base; and in the case where the P¹ group is a Teoc group, a reagent that forms a fluoride ion such as tetrabutylammonium fluoride can be used. In the case where the P¹ group is an alkoxycarbonyl group such as a methoxycarbonyl group or an ethoxycarbonyl group, it may be performed by heating in the presence of an organic amine such as triethylamine or diisopropylethylamine (DIPEA), or an inorganic base such as potassium carbonate or sodium carbonate.

The compound (I) obtained by step 3 can be converted to a pharmacologically acceptable salt thereof by a method well known to those skilled in the art.

<Production Method 2 for Compound (I)>

Production method 2 is a method for obtaining compound (D) through steps 4 and 5 with compound (C) as a starting material, followed by conversion to compound (1) according to step 3 of production method 1 described above. Production method 2 is a suitable production method in the case where L² is an oxygen atom or an optionally substituted nitrogen atom. In production method 2, R¹, R², R³, R⁴, R⁵, L¹, L², L³, P¹, and X are defined as in production method 1 described above.

(Step 4)

Step 4 is the step of reacting compound (C) with an acylating agent to obtain compound (E).

In step 4, the L² group is an oxygen atom or an optionally substituted nitrogen atom. Specifically, the compound (C) is an alcohol or an amine.

As the acylating agent, for example, phosgene, diphosgene, triphosgene, carbonyldiimidazole (CDI), N,N′-disuccinimidyl carbonate, or carbonic acid ester can be used.

The amount of the acylating agent used is preferably 1 to 5 mol, more preferably 1 to 2 mol, with respect to 1 mol of the compound (C).

The reaction of step 4 may be performed in a solvent or may be performed without a solvent. In the case of using a solvent, there is no limitation as long as the solvent does not have influence on the reaction, and an organic solvent is preferred. Examples of the organic solvent include acetonitrile, dichloromethane, diethyl ether, tetrahydrofuran (THF), N,N-dimethylformamide (DMF), and dimethyl sulfoxide (DMSO).

In step 4, a base can be further added in order to accelerate the reaction. Examples of the base include organic amines such as triethylamine, diisopropylethylamine (DIPEA), 1,5-diazabicyclo[4.3.0]nonene (DBN), 1,8-diazabicyclo[5.4.0]undecene (DBU), pyridine, and 4-dimethylaminopyridine (DMAP).

The amount of the base added is preferably 1 to 5 mol, more preferably 1 to 2 mol, with respect to 1 mol of the compound (C).

The reaction temperature of step 4 can be appropriately set by those skilled in the art. The reaction temperature is usually 0 to 100° C., preferably 20 to 40° C.

(Step 5)

Step 5 is the step of reacting compound (E) with compound (A) to obtain compound (D).

The amount of the compound (E) used is preferably 1 to 5 mol, more preferably 1 to 2 mol, with respect to 1 mol of the compound (A). The compound (E) and the compound (A) may be dissolved in an organic solvent and added to the reaction solution.

The reaction of step 5 may be performed in a solvent or may be performed without a solvent. In the case of using a solvent, there is no limitation as long as the solvent does not have influence on the reaction, and an organic solvent is preferred. Examples of the organic solvent include dichloromethane, diethyl ether, tetrahydrofuran (THF), N,N-dimethylformamide (DMF), and dimethyl sulfoxide (DMSO).

In step 5, a base can be further added in order to accelerate the reaction. Examples of the base include organic amines such as triethylamine, diisopropylethylamine (DIPEA), 1,5-diazabicyclo[4.3.0]nonene (DBN), 1,8-diazabicyclo[5.4.0]undecene (DBU), pyridine, and 4-dimethylaminopyridine (DMAP).

The amount of the base added is preferably 1 to 10 mol, more preferably 1 to 5 mol, with respect to 1 mol of the compound (A).

The reaction temperature of step 5 can be appropriately set by those skilled in the art. The reaction temperature is usually 0 to 100° C., preferably 20 to 40° C.

<Production Method 3 for Compound (I)>

Production method 3 is a method for reacting compound (A) with compound (F) to obtain compound (D), followed by conversion to compound (I) according to step 3 of production method 1 described above. Production method 3 is a suitable production method in the case where L² is a single bond, an optionally substituted linear or branched C₁₋₆ alkylene group, an optionally substituted linear or branched C₂₋₆ alkenylene group, an optionally substituted linear or branched C₂₋₆ alkynylene group, an optionally substituted C₃₋₆ cycloalkylene group, or an optionally substituted C₃₋₆ cycloalkenylene group. In production method 3, R¹, R², R³, R⁴, R⁵, L¹, L³, and P¹ are defined as in production method 1 described above.

(Step 6)

Step 6 is the step of condensing compound (A) with compound (F) to obtain compound (D). The condensation reaction involves converting the compound (F) to an acid halide, a carboxylic anhydride, an acid azide, or an active ester by using a reagent used in amide bond formation reaction, followed by reaction with the compound (A). The reagent used in amide bond formation reaction is not particularly limited as long as being a reagent known as a reagent used in amide bond formation reaction to those skilled in the art.

The amount of the compound (F) used is preferably 1 to 10 mol, more preferably 1 to 5 mol, with respect to 1 mol of the compound (A). The compound (F) may be dissolved in an organic solvent and added to the reaction solution.

The reaction of step 6 may be performed in a solvent or may be performed without a solvent. In the case of using a solvent, there is no limitation as long as the solvent does not have influence on the reaction, and an organic solvent is preferred. Examples of the organic solvent include dichloromethane, 1,2-dichloroethane, diethyl ether, tetrahydrofuran (THF), N,N-dimethylformamide (DMF), and dimethyl sulfoxide (DMSO).

In step 6, a base can be further added in order to accelerate the reaction. Examples of the base include organic amines such as triethylamine, diisopropylethylamine (DIPEA), 1,5-diazabicyclo[4.3.0]nonene (DBN), 1,8-diazabicyclo[5.4.0]undecene (DBU), pyridine, and 4-dimethylaminopyridine (DMAP).

The amount of the base added is preferably 1 to 10 mol, more preferably 1 to 5 mol, with respect to 1 mol of the compound (A).

The reaction temperature of step 6 can be appropriately set by those skilled in the art. The reaction temperature is usually 0 to 100° C., preferably 20 to 40° C.

<Production Method 4 for Compound (I)>

Production method 4 is a method for obtaining compound (D) through step 7 and step 8 with compound (H) as a starting material, followed by conversion to compound (I) according to step 3 of production method 1 described above. In production method 4, R¹, R², R³, R⁴, L¹, L², and L³ are defined as in formula (I). P¹ group is a protective group for the amino group, and P² is a protective group for the hydroxy group. The P¹ group is defined as in production method 1 described above.

The P² group is not particularly limited as long as being a substituent known as a protective group for the hydroxy group to those skilled in the art. Examples of the P² group include: optionally substituted C₇₋₁₁ aralkyl groups such as a benzyl group, a p-methoxyphenylmethyl group, and a o-nitrophenylmethyl group; optionally substituted acyl groups such as an acetyl group, a trifluoroacetyl group, and a benzoyl group; and substituted silyl groups such as a trimethylsilyl group, a tert-butyldimethylsilyl group, a triethylsilyl group, a triisopropylsilyl group, and a tert-butyldiphenylsilyl group.

(Step 7)

Step 7 is the step of performing the deprotection reaction of compound (H) to obtain compound (J). The removal reaction of the P² group can also be performed by a method well known to those skilled in the art (e.g., a method described in, for example, Protective Groups in Organic Synthesis, 4th ed., T. W. Greene, P. G. M. Wuts, John Wiley & Sons Inc. (2006)).

(Step 8)

Step 8 is the step of reacting compound (J) with an acid halide, an acid anhydride, or an alkyl halide to obtain compound (D).

The amount of the acid halide, the acid anhydride, or the alkyl halide used is preferably 1 to 10 mol, more preferably 1 to 2 mol, with respect to 1 mol of the compound (J).

The reaction of step 7 may be performed in a solvent or may be performed without a solvent. In the case of using a solvent, there is no limitation as long as the solvent does not have influence on the reaction, and an organic solvent is preferred. Examples of the organic solvent include dichloromethane, diethyl ether, tetrahydrofuran (THF), 1,4-dioxane, N,N-dimethylformamide (DMF), and dimethyl sulfoxide (DMSO).

In step 8, a base can be further added in order to accelerate the reaction. Examples of the base include organic amines such as triethylamine, diisopropylethylamine (DIPEA), 1,5-diazabicyclo[4.3.0]nonene (DBN), 1,8-diazabicyclo[5.4.0]undecene (DBU), pyridine, and 4-dimethylaminopyridine (DMAP).

The amount of the base added is preferably 1 to 20 mol, more preferably 1 to 5 mol, with respect to 1 mol of the compound (J).

The reaction temperature of step 8 can be appropriately set by those skilled in the art. The reaction temperature is usually −20 to 120° C., preferably 15 to 100° C.

<Method for Producing Compound (A)>

The compound (A) can be produced, for example, by the following method with compound (A1) as a starting material. Compound (A1) can be produced, for example, with reference to WO2007/72153 or through the following steps 11 to 15.

The compound (A1) is 3-amino-6,6-dimethyl-4,6-dihydropyrrolo[3,4-c]pyrazole in which the nitrogen atom on the pyrazole skeleton may be substituted by P¹ group, and the nitrogen atom at 5-position may be substituted by P³ group. The P¹ group can substitute an acidic proton of pyrazole in the 4,6-dihydropyrrolo[3,4-c]pyrazole skeleton. Thus, the P¹ group may be added to position 1 of the 4,6-dihydropyrrolo[3,4-c]pyrazole skeleton or may be added to 2-position. Compound (A1) and compound (A2) will be described by using a chemical formula wherein it is added to 1-position of the 4,6-dihydropyrrolo[3,4-c]pyrazole skeleton, for the sake of convenience.

In the compound (A1), P¹ has the same meaning as defined in compound (A). The P³ group is not particularly limited as long as being a substituent known as a protective group for the amino group to those skilled in the art. Examples of the P³ group include: optionally substituted C₇₋₁₁ aralkyl groups such as a benzyl group, a p-methoxyphenylmethyl group, and a o-nitrophenylmethyl group; optionally substituted C₁₋₆ alkylcarbonyl groups such as an acetyl group and a trifluoroacetyl group; optionally substituted C₆₋₁₀ arylcarbonyl groups such as a benzoyl group; optionally substituted C₁₋₆ alkoxycarbonyl groups such as a methoxycarbonyl group, an ethoxycarbonyl group, a Boc group (tert-butoxycarbonyl group), a Cbz group (benzyloxycarbonyl group), a Fmoc group (fluorenylmethyloxycarbonyl group), and a Teoc group (trimethylsilylethyloxycarbonyl group); alkenyloxycarbonyl groups such as an Alloc group (allyloxycarbonyl group); alkylsulfonyl groups such as a methanesulfonyl group; and optionally substituted C₆₋₁₀ arylsulfonyl groups such as a p-toluenesulfonyl group.

In the formulas (A2) and (A3), R¹, R², R³, and L¹ have the same meanings as defined in compound (I). The group X is not particularly limited as long as being a substituent known as a leaving group to those skilled in the art. Examples of X include: halogen atoms; an imidazolyl group; aminooxy groups such as a succinyl-N-oxy group and a benzotriazolyl-N-oxy group; and acyloxy groups such as a pivaloyloxy group and a benzoyloxy group. Alternatively, X may be a hydroxy group.

In the case where the compound (A2) is a carboxylic acid (i.e., X is a hydroxy group), it may be converted to an acid anhydride by a method well known to those skilled in the art and then reacted with the compound (A1), or may be reacted with the compound (A1) by using a reagent known as a condensing agent used in amide bond formation reaction to those skilled in the art.

(Step 9)

Step 9 is the step of reacting compound (A1) with compound (A2) to obtain compound (A3).

The amount of the compound (A2) used is preferably 1 to 10 mol, more preferably 1 to 3 mol, with respect to 1 mol of the compound (A1).

The reaction of step 9 may be performed in a solvent or may be performed without a solvent. In the case of using a solvent, there is no limitation as long as the solvent does not have influence on the reaction, and an organic solvent is preferred. Examples of the organic solvent include dichloromethane, diethyl ether, tetrahydrofuran (THF), N,N-dimethylformamide (DMF), and dimethyl sulfoxide (DMSO).

In step 9, a base can be further added in order to accelerate the reaction. Examples of the base include organic amines such as triethylamine, diisopropylethylamine (DIPEA), 1,5-diazabicyclo[4.3.0]nonene (DBN), 1,8-diazabicyclo[5.4.0]undecene (DBU), pyridine, and 4-dimethylaminopyridine (DMAP).

The amount of the base added is preferably 1 to 20 mol, more preferably 1 to 5 mol, with respect to 1 mol of the compound (A1).

The reaction temperature of step 9 can be appropriately set by those skilled in the art. The reaction temperature is usually −40 to 100° C., preferably −20 to 20° C.

(Step 10)

Step 10 is the step of performing the deprotection reaction of compound (A3) to obtain compound (A). The removal reaction of the P³ group can also be performed by a method well known to those skilled in the art (e.g., a method described in, for example, Protective Groups in Organic Synthesis, 4th ed., T. W. Greene, P. G. M. Wuts, John Wiley & Sons Inc. (2006)).

<Method for Producing Compound (A1)>

In the formulas (A6), (A7), and (A8), P³ has the same meaning as defined in compound (A1).

(Step 11)

Step 11 is the step of reacting compound (A4) with acrylonitrile to obtain compound (A5).

The amount of the acrylonitrile used is preferably 1 to 10 mol, more preferably 1 to 3 mol, with respect to 1 mol of the compound (A4).

In step 11, there is no limitation as long as a solvent does not have influence on the reaction, and an aqueous solvent is preferred.

In step 11, a base can be further added in order to accelerate the reaction. Examples of the base include inorganic bases such as potassium hydroxide. The amount of the base added is preferably 0.8 to 2 mol, with respect to 1 mol of the compound (A1).

The reaction temperature of step 11 can be appropriately set by those skilled in the art. The reaction temperature is usually 0 to 100° C., preferably 50 to 90° C.

(Step 12)

Step 12 is the step of protecting the amino group of compound (A5) with P³ group to obtain compound (A6). The protection reaction of the amino group with the P³ group can be performed by a method well known to those skilled in the art (e.g., a method described in, for example, Protective Groups in Organic Synthesis, 4th ed., T. W. Greene, P. G. M. Wuts, John Wiley & Sons Inc. (2006)).

(Step 13)

Step 13 is the step of performing the cyclization reaction of compound (A6) to obtain compound (A7).

The reaction of step 13 may be performed in a solvent or may be performed without a solvent. In the case of using a solvent, there is no limitation as long as the solvent does not have influence on the reaction, and an organic solvent is preferred. Examples of the organic solvent include diethyl ether, tetrahydrofuran (THF), 1,4-dioxane, N,N-dimethylformamide (DMF) toluene.

In step 13, a base can be further added in order to accelerate the reaction. Examples of the base include sodium hydride, potassium hydride, sodium methoxide, sodium ethoxide, n-butyllithium, and tert-butoxy potassium. The amount of the base added is preferably 1 to 3 mol with respect to 1 mol of the compound (A6).

The reaction temperature of step 13 can be appropriately set by those skilled in the art. The reaction temperature is usually 20 to 150° C., preferably 50 to 100° C.

(Step 14)

Step 14 is the step of reacting compound (A7) with hydrazine to obtain compound (A8).

The reaction of step 14 may be performed in a solvent or may be performed without a solvent. In the case of using a solvent, there is no limitation as long as the solvent does not have influence on the reaction, and an organic solvent is preferred. Examples of the organic solvent include ethanol, n-propanol, and n-butanol.

In step 14, an acid can be further added in order to accelerate the reaction. Examples of the acid include acetic acid, hydrochloric acid, and sulfuric acid. The amount of the acid added is preferably 1 to 10 mol with respect to 1 mol of the compound (A7).

The reaction temperature of step 14 can be appropriately set by those skilled in the art. The reaction temperature is usually 20 to 150° C., preferably 50 to 120° C.

(Step 15)

Step 15 is the step of protecting the amino group of compound (A7) with P¹ group to obtain compound (A1). The protection reaction of the amino group with the P¹ group can be performed by a method well known to those skilled in the art (e.g., a method described in, for example, Protective Groups in Organic Synthesis, 4th ed., T. W. Greene, P. G. M. Wuts, John Wiley & Sons Inc. (2006)).

EXAMPLE

Hereinafter, the present invention will be described further specifically as to the compound according to the present embodiment or the pharmaceutically acceptable salt thereof by showing Examples (Examples 1 to 125), Reference Examples (Reference Examples 1 to 137), and Test Examples (Test Examples 1 to 12); however, these examples are given for more understanding the present invention and does not limit the scope of the present invention.

DIOL silica gel in silica gel column chromatography represents CHROMATOREX (trade name) DIOL MB 100-40/75 manufactured by Fuji Silysia Chemical Ltd.

DNH silica gel in silica gel column chromatography represents CHROMATOREX (trade name) DNH MB 100-40/75 manufactured by Fuji Silysia Chemical Ltd.

In the case where a plurality of values of mass spectra are observed due to the presence of isotopes, only one having minimum m/z was described. DUIS in an ionization mode of a mass spectrum is a mixed mode of ESI and APCI.

¹H-NMR is indicated by chemical shift (δ) with tetramethylsilane as an internal standard (0 ppm), and a coupling constant (J value) is indicated by Hz unit, unless otherwise specified. An abbreviation for the split pattern of each peak has the following meaning: s: singlet, d: doublet, t: triplet, q: quartet, and br: broad.

Abbreviations described in Examples and Reference Examples are usually used as meanings generally used in the fields of organic chemistry and pharmacy. Each abbreviation is specifically understood by those skilled in the art as follows.

ATP: adenosine triphosphate

Boc: tert-butyloxycarbonyl

DIPEA: N,N-diisopropylethylamine

DMF: N,N-dimethylformamide

DMSO: dimethyl sulfoxide

DTT: dithiothreitol

Et: ethyl

FBS: fetal bovine serum

HEPES: N-2-hydroxyethylpiperazine-N′-2-ethanesulfonic acid

MBP: myelin basic protein

n-: normal

NADPH: nicotinamide adenine dinucleotide phosphate

PBMC: peripheral blood mononuclear cell

PBS: aqueous solution of phosphate-buffered sodium chloride

TBME: tert-butyl methyl ether

TB S: tert-butyldimethylsilyl

tert-: tertiary

THF: tetrahydrofuran

Tris: trishydroxyaminomethane

Example 1 (S)—N-(2-Hydroxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-114)

To a solution of 308 mg (0.698 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 6 ml of THF, 0.23 ml (1.4 mmol) of DIPEA and 472 mg (3.44 mmol) of (S)-(+)-2-phenylglycinol were added at room temperature, then applied to a microwave reaction apparatus, and reacted at 80° C. for 1 hour. Subsequently, 2.7 ml (67 mmol) of methanol and 2.7 ml (19 mmol) of triethylamine were added to the reaction solution, then applied to a microwave reaction apparatus, and reacted at 80° C. for 0.5 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 98:2 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with ethyl acetate/diethyl ether, and the obtained solid was collected by filtration. 20 ml of water was added to the obtained solid and stirred, and then, insoluble matter was collected by filtration and dried under reduced pressure to obtain 152 mg of the title compound (yield: 46%) as a white solid.

Mass spectrum (DUIS, m/z): 470 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.65 (br s, total 1H), 9.66-9.46 (m, 1H), 7.41-7.25 (m, 4H), 7.22-7.15 (m, 1H), 6.18 & 6.06 (d, J=7.7 Hz, total 1H), 4.88 (t, J=5.9 Hz, 1H), 4.83-4.71 (m, 1H), 4.62-4.41 (m, 2H), 3.69-3.52 (m, 2H), 2.49-2.41 (m, 2H), 2.30-2.12 (m, 2H), 1.93-1.73 (m, 2H), 1.68-1.44 (m, 6H), 0.17-0.04 (m, 9H).

Example 2 (S)—N-(2-Hydroxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. III-114)

To a solution of 433 mg (1.08 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate hydrochloride synthesized in the similar manner as in Reference Example 7 in 7.5 ml of dehydrated dichloromethane, 0.90 ml (5.2 mmol) of DIPEA was added at room temperature in a nitrogen atmosphere, and then, a solution of 275 mg (0.928 mmol) of bis(trichloromethyl)carbonate in 2.5 ml of dehydrated dichloromethane was added dropwise at −78° C. and stirred at the same temperature as above for 2.5 hours.

After the completion of the reaction, 10 ml of a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred while the temperature was raised to room temperature for a while. The organic layer and the aqueous layer were separated, and then, the aqueous layer was subjected to extraction with dichloromethane twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 80:20 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain a concentration residue.

To a solution of 457 mg of the obtained concentration residue in 4 ml of dehydrated THF, 0.40 ml (2.2 mmol) of DIPEA and 528 mg (3.85 mmol) of (S)-(+)-2-phenylglycinol were added at room temperature in a nitrogen atmosphere and then stirred for 3.75 hours while heated to reflux. Subsequently, 0.90 ml (6.5 mmol) of triethylamine and 0.90 ml (22 mmol) of methanol were added to the reaction solution and then stirred for 1 hour while heated to reflux.

After the completion of the reaction, water was added to the reaction solution, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DNH silica gel, elution solvent: dichloromethane:methanol=100:0 to 97:3 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with ethyl acetate/diisopropyl ether/n-hexane, and the deposited solid was collected by filtration, washed by sousing with n-hexane, and then dried under reduced pressure to obtain 388 mg of the title compound (yield: 79% [2 steps]) as a white solid.

Mass spectrum (CI, m/z): 456 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.02 & 11.54 (br s, total 1H), 9.44 & 9.25 (br s, total 1H), 7.40-7.33 (m, 2H), 7.33-7.24 (m, 2H), 7.23-7.16 (m, 1H), 5.88-5.69 (m, 1H), 4.86-4.79 (m, 1H), 4.61 (t, J=5.6 Hz, 1H), 4.55-4.37 (m, 2H), 3.71-3.64 (m, 2H), 1.63 (s, 3H), 1.57 (s, 3H), 1.08-1.01 (m, 2H), 0.83-0.60 (m, 2H), 0.07 (s, 9H).

Example 3 (S)—N-(2-Hydroxy-1-phenylethyl)-6,6-dimethyl-3-[2-methyl-2-(trimethylsilyl)propanamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. II-114)

To a solution of 337 mg (0.714 mmol) of 5-tert-butyl 1-ethyl 6,6-dimethyl-3-[2-methyl-2-(trimethylsilyl)propanamido]pyrrolo[3,4-c]pyrazole-1,5(4H,6H)-dicarboxylate synthesized in the similar manner as in Reference Example 9 in 3 ml of dehydrated dichloromethane, 0.25 ml (2.2 mmol) of 2,6-lutidine and 0.39 ml (2.2 mmol) of trimethylsilyl trifluoromethanesulfonate were added in this order at 0° C. in a nitrogen atmosphere and stirred at the same temperature as above for 1.5 hours.

After the completion of the reaction, the reaction solution was diluted with dichloromethane and subsequently washed with a saturated aqueous solution of sodium bicarbonate. The organic layer and the aqueous layer were separated, and then, the aqueous layer was subjected to extraction with dichloromethane twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The operation of adding 25 ml of toluene to the obtained concentration residue and concentrating it under reduced pressure was repeated three times, followed by drying under reduced pressure to obtain a concentration residue.

To a solution of 292 mg of the obtained concentration residue in 5 ml of dehydrated dichloromethane, 0.38 ml (2.2 mmol) of DIPEA was added at room temperature in a nitrogen atmosphere, and then, 149 mg (0.502 mmol) of bis(trichloromethyl)carbonate was added at −78° C. and stirred at the same temperature as above for 2.5 hours.

After the completion of the reaction, 7 ml of a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred while the temperature was raised to room temperature for a while. The organic layer and the aqueous layer were separated, and then, the aqueous layer was subjected to extraction with dichloromethane once. All of the organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 85:15 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain a concentration residue.

To a solution of 262 mg of the obtained concentration residue in 3 ml of dehydrated THF, 0.27 ml (1.6 mmol) of DIPEA and 255 mg (1.86 mmol) of (S)-(+)-2-phenylglycinol were added at room temperature in a nitrogen atmosphere and then stirred for 2.5 hours while heated to reflux. Subsequently, 1.0 ml (7.2 mmol) of triethylamine and 1.0 ml (25 mmol) of methanol were added to the reaction solution and then stirred for 5.5 hours while heated to reflux.

After the completion of the reaction, water was added to the reaction solution, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. 0.10 ml of acetic acid was added to the obtained concentration residue and then subjected to silica gel column chromatography (DIOL silica gel, elution solvent: dichloromethane:methanol=100:0 to 97:3 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with ethyl acetate/n-hexane, and the obtained solid was collected by filtration, washed by sousing with n-hexane, and then dried under reduced pressure to obtain 206 mg of the title compound (yield: 63% [3 steps]) as a pale yellow solid.

Mass spectrum (CI, m/z): 458 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.25 & 11.64 (br s, total 1H), 9.42-9.11 (m, 1H), 7.38-7.25 (m, 4H), 7.23-7.15 (m, 1H), 6.21-6.05 (m, 1H), 4.87 (t, J=5.9 Hz, 1H), 4.81-4.73 (m, 1H), 4.57-4.41 (m, 2H), 3.70-3.54 (m, 2H), 1.66-1.47 (m, 6H), 1.25 (s, 6H), 0.04 (s, 9H).

Example 4 (S)-3-[1-(Ethyldimethylsilyl)cyclobutanecarboxamido]-N-(2-hydroxy-1-phenylethyl)-6,6-dimethyl-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-117)

To a solution of 454 mg (0.997 mmol) of ethyl 5-(chlorocarbonyl)-3-[1-(ethyldimethylsilyl)cyclobutanecarboxamido]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 13 in 10 ml of dehydrated THF, 700 mg (5.10 mmol) of (S)-(+)-2-phenylglycinol and 0.35 ml (2.0 mmol) of DIPEA were added at room temperature in an argon atmosphere and then stirred at 60° C. for 4 hours. Subsequently, 6 ml of methanol and 2 ml of triethylamine were added to the reaction solution and stirred at 60° C. for 2 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, a saturated aqueous solution of sodium bicarbonate was added to the obtained concentration residue, and the mixed solution was subjected to extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 98:2 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the concentration residue, crystallization was performed with dichloromethane/diisopropyl ether, and the deposited solid was collected by filtration and subsequently dried under reduced pressure to obtain 404 mg of the title compound (yield: 84%) as a white solid.

Mass spectrum (DUIS, m/z): 484 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.66 (br s, total 1H), 9.64-9.47 (m, 1H), 7.40-7.14 (m, 5H), 6.26-6.01 (m, 1H), 4.88 (t, J=5.8 Hz, 1H), 4.83-4.71 (m, 1H), 4.60-4.43 (m, 2H), 3.66-3.54 (m, 2H), 2.48-2.42 (m, 2H), 2.33-2.14 (m, 2H), 1.93-1.72 (m, 2H), 1.67-1.45 (m, 6H), 0.92 (t, J=7.9 Hz, 3H), 0.60 (q, J=7.9 Hz, 2H), 0.08 (s, 6H).

Example 5 (S)-3-[2-(Ethyldimethylsilyl)-2-methylpropanamido]-N-(2-hydroxy-1-phenylethyl)-6,6-dimethyl-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. II-116)

To a solution of 2.44 g (6.41 mmol) of ethyl 3-[2-(ethyldimethylsilyl)-2-methylpropanamido]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate synthesized in the similar manner as in Reference Example 16 in 30 ml of dehydrated dichloromethane, 5.6 ml (32 mmol) of DIPEA and a solution of 1.33 g (4.48 mmol) of bis(trichloromethyl)carbonate in 10 ml of dehydrated dichloromethane were added in this order at −78° C. in a nitrogen atmosphere and stirred at the same temperature as above for 1 hour.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, and the temperature was raised to room temperature for a while with stirring. After separation into an aqueous layer and an organic layer, the aqueous layer was subjected to extraction with dichloromethane. All of the obtained organic layers were dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=95:5 to 70:30 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 2.51 g of a concentration residue.

To a solution of 474 mg of the obtained concentration residue in ml of dehydrated THF, 700 mg (5.10 mmol) of (S)-2-amino-2-phenylethanol and 0.35 ml (2.0 mmol) of DIPEA were added at room temperature in an argon atmosphere, then applied to a microwave reaction apparatus, and reacted at 100° C. for 2 hours. After standing to cool, 6 ml of methanol and 2 ml of triethylamine were added, applied to a microwave reaction apparatus, and reacted at 80° C. for 3 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, a saturated aqueous solution of sodium bicarbonate was added to the obtained concentration residue, and the mixed solution was subjected to extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 98:2 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the concentration residue, crystallization was performed with dichloromethane/diisopropyl ether, and the deposited solid was collected by filtration and subsequently dried under reduced pressure to obtain 321 mg of the title compound (yield: 56% [2 steps]) as a white solid.

Mass spectrum (DUIS, m/z): 472 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.26 & 11.67 (br s, total 1H), 9.42-9.16 (m, 1H), 7.38-7.25 (m, 4H), 7.25-7.14 (m, 1H), 6.20-6.04 (m, 1H), 4.88 (t, J=5.8 Hz, 1H), 4.82-4.72 (m, 1H), 4.55-4.42 (m, 2H), 3.66-3.55 (m, 2H), 1.64-1.48 (m, 6H), 1.26 (s, 6H), 0.90 (t, J=7.9 Hz, 3H), 0.56 (q, J=7.9 Hz, 2H), 0.02 (s, 6H).

Example 6 (S)—N-(2-Hydroxy-1-phenylethyl)-N,6,6-trimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-119)

To a solution of 210 mg (1.39 mmol) of (S)-2-(methylamino)-2-phenylethanol [synthesized according to the method described in J. Org. Chem., 1992, 57, 5383-5394] in 3 ml of dehydrated 1,4-dioxane, 0.24 ml (1.37 mmol) of DIPEA and 200 mg (0.454 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 were added in an argon atmosphere and stirred at 100° C. for 3 hours. Subsequently, 1 ml of triethylamine and 1 ml of methanol were added to the reaction solution and stirred at room temperature for 16 hours.

After the completion of the reaction, water was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=50:50 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was repulp-washed in hexane, and the solid was collected by filtration and then dried under reduced pressure to obtain 105 mg of the title compound (yield: 48%) as a white solid.

Mass spectrum (CI, m/z): 484 [M+1]⁺

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.84 (br s, total 1H), 9.75-9.42 (m, 1H), 7.41-7.21 (m, 5H), 4.85 (t, J=5.2 Hz, 1H), 4.82-4.76 (m, 1H), 4.58-4.35 (m, 2H), 3.96-3.78 (m, 2H), 2.52 (s, 3H), 2.47-2.38 (m, 2H), 2.23-2.11 (m, 2H), 1.87-1.72 (m, 2H), 1.71-1.52 (m, 6H), 0.05 (s, 9H).

Example 7 (S)-2-[(2-Methoxypropan-2-yl)oxy]-1-phenylethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate (Compound No. VI-360)

To 205 mg of crude ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate [containing impurities] obtained through the same reaction as in Reference Example 5 from 225 mg (0.470 mmol) of 5-tert-butyl 1-ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]pyrrolo[3,4-c]pyrazole-1,5(4H,6H)-dicarboxylate synthesized in the similar manner as in Reference Example 4, a solution of 187 mg (0.533 mmol) of (S)-2,5-dioxopyrrolidin-1-yl {2-[(2-methoxypropan-2-yl)oxy]-1-phenylethyl}carbonate synthesized in the similar manner as in Reference Example 18 in 3 ml of THF and 0.28 ml (1.6 mmol) of DIPEA were added at room temperature in a nitrogen atmosphere and stirred at the same temperature as above for 15 hours. Subsequently, 1.0 ml (7.2 mmol) of triethylamine and 0.70 ml (17 mmol) of methanol were added to the reaction solution and stirred at room temperature 4.5 hours and for 2 hours while heated to reflux, and then, 247 mg (1.80 mmol) of (S)-2-amino-2-phenylethanol was added to the reaction solution and stirred for 4.5 hours while heated to reflux.

After the completion of the reaction, water was added to the reaction solution, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=80:20 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with ethyl acetate/n-hexane, and the deposited solid was collected by filtration, washed by sousing with n-hexane, and then dried under reduced pressure to obtain 22.7 mg of the title compound (yield: 9% [2 steps]) as a white solid. The filtrate was further concentrated under reduced pressure and dried under reduced pressure to obtain 178 mg of the title compound (yield: 70% [2 steps]) as a white foam.

Mass spectrum (ESI, m/z): 565 [M+23(Na)]⁺, 541 [M−1]⁻.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.35-12.19 & 11.96-11.80 (m, total 1H), 9.85-9.44 (m, 1H), 7.45-7.26 (m, 5H), 5.81-5.68 (m, 1H), 4.63-4.18 (m, 2H), 3.72-3.50 (m, 2H), 3.08-2.94 (m, 3H), 2.56-2.38 (m, 2H), 2.30-2.10 (m, 2H), 1.94-1.75 (m, 2H), 1.73-1.45 (m, 6H), 1.32-1.18 (m, 6H), 0.13-0.02 (m, 9H).

Example 8 (S)-2-Hydroxy-1-phenylethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate (Compound No. IV-2)

To a solution of 175 mg (0.322 mmol) of (S)-2-[(2-methoxypropan-2-yl)oxy]-1-phenylethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate synthesized in the similar manner as in Example 7 in 2.5 ml of methanol, 9.6 mg (0.038 mmol) of pyridinium p-toluenesulfonate was added at 0° C. in a nitrogen atmosphere and stirred at the same temperature as above for 70 minutes.

After the completion of the reaction, 0.1 ml of triethylamine was added to the reaction solution and then concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=65:35 to 25:75 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with ethyl acetate/n-hexane, and the deposited solid was collected by filtration, washed by sousing with n-hexane, and then dried under reduced pressure to obtain 124 mg of the title compound (yield: 82%) as a white solid.

Mass spectrum (CI, m/z): 471 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.35-12.11 & 11.97-11.79 (m, total 1H), 9.84-9.46 (m, 1H), 7.46-7.20 (m, 5H), 5.71-5.58 (m, 1H), 5.12-4.95 (m, 1H), 4.72-4.18 (m, 2H), 3.80-3.54 (m, 2H), 2.60-2.38 (m, 2H), 2.30-2.10 (m, 2H), 1.93-1.74 (m, 2H), 1.74-1.43 (m, 6H), 0.16-0.02 (m, 9H).

Example 9 2-Methoxy-1-phenylethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate (Compound No. III-5)

To a solution of 2.15 g (5.36 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate hydrochloride synthesized in the similar manner as in Reference Example 7 in 72 ml of dehydrated dichloromethane, 3.6 ml (21 mmol) of DIPEA was added at room temperature and subsequently cooled in a dry ice/acetone coolant, and then, a solution of 1.17 g (3.94 mmol) of bis(trichloromethyl)carbonate in 12 ml of dehydrated dichloromethane was added dropwise over 30 minutes and stirred at the same temperature as above for 6 hours. During this reaction, 3.6 ml (21 mmol) of DIPEA 4 times and DIPEA (1.0 ml, 5.7 mmol) once were added in this order.

After the completion of the reaction, 46 ml of a saturated aqueous solution of sodium bicarbonate was added at −78° C., and then, the temperature was raised to room temperature for a while. The reaction solution was separated into an aqueous layer and an organic layer, then the aqueous layer was subjected to extraction with 50 ml of dichloromethane twice, all of the obtained organic layers were dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=78:22 to 57:43 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. 20 ml of n-hexane was added to the concentration residue and cooled in ice, and then, the deposited solid was collected by filtration and dried under reduced pressure to obtain 1.96 g of white solid.

To 40.4 mg (0.0946 mmol) of the obtained white solid, 224 mg (1.48 mmol) of 2-methoxy-1-phenylethanol [synthesized according to the method described in WO 2012/138648], 26.0 mg (0.188 mmol) of potassium carbonate, 0.8 ml of 1,2-dimethoxyethane, and 80 mg of molecular sieve 4 A (powder) were added at room temperature and then stirred at 80° C. for 26 hours.

After the completion of the reaction, insoluble matter was filtered, and 10 ml of ethyl acetate, 5 ml of water, and 5 ml of a saturated aqueous solution of sodium chloride were added to the filtrate and then the aqueous layer and the organic layer were separated. The obtained organic layer was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography four times (silica gel (1st run), elution solvent: 1,2-dichloroethane:methanol=100:0 to 93:7 (V/V); silica gel (2nd run), elution solvent: ethyl acetate:methanol=98:2 to 95:5 (V/V); silica gel (3rd run), elution solvent: 1,2-dichloroethane:methanol=98:2 to 95:5 (V/V); and DNH silica gel, elution solvent: 1,2-dichloroethane:methanol=98:2 to 95:5 (V/V)) and preparative HPLC (column: X-Bridge (trade name) ODS, elution solvent: 0.1% aqueous formic acid solution: 0.1% formic acid:acetonitrile=50:50 to 5:95 (V/V))), and a fraction containing the compound of interest was neutralized with dilute aqueous ammonia solution and then concentrated under reduced pressure. The obtained concentration residue was dissolved by adding acetonitrile and water and then freeze-dried to obtain 4.1 mg of the title compound (yield: 8% [2 steps]) as a white foam.

Mass spectrum (DUIS, m/z): 471 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.40-11.86 (m, 1H), 10.11-9.61 (m, 1H), 7.49-7.22 (m, 5H), 5.90-5.71 (m, 1H), 4.63-4.14 (m, 2H), 3.77-3.51 (m, 2H), 3.30-3.29 (m, 3H), 1.78-1.40 (m, 6H), 1.11-0.92 (m, 2H), 0.81-0.59 (m, 2H), 0.11-0.04 (m, 9H).

Example 10 N-[5-(4-Hydroxy-3-phenylbutanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-558)

To a solution of 160 mg (0.536 mmol) of ethyl 4-(benzyloxy)-3-phenylbutanoate synthesized in the similar manner as in Reference Example 19 in a mixture of 3 ml of THF/1.5 ml of water, 48 mg (1.1 mmol) of lithium hydroxide monohydrate was added at room temperature in an argon atmosphere, stirred at the same temperature as above for 2 hours, and then stirred at 60° C. for 3 hours. The reaction solution was concentrated under reduced pressure, and 3 ml of ethanol and 1.0 ml (2.0 mmol) of a 2 N aqueous sodium hydroxide solution were added to the obtained concentration residue at room temperature and heated and stirred at 60° C. for 1 hour.

After the completion of the reaction, 1 N hydrochloric acid was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 50:50 (V/V)), and a fraction containing 4-(benzyloxy)-3-phenylbutanoic acid was concentrated under reduced pressure and dried under reduced pressure to obtain a concentration residue.

To a solution of 137 mg of the obtained concentration residue, 165 mg (0.436 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate synthesized in the similar manner as in Reference Example 5, and 201 mg (0.529 mmol) of O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate in 3 ml of dehydrated dichloromethane, 0.185 ml (1.06 mmol) of DIPEA was added at room temperature in an argon atmosphere and stirred at room temperature for 16 hours.

After the completion of the reaction, water was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=70:30 to 0:100 (V/V)), and a fraction containing ethyl 5-[4-(benzyloxy)-3-phenylbutanoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-1 (4H)-carboxylate was concentrated under reduced pressure and dried under reduced pressure to obtain a concentration residue.

To a solution of 256 mg of the obtained concentration residue in a mixture of 2 ml of THF/2 ml of methanol, 2 ml of triethylamine was added at room temperature in an argon atmosphere and stirred at the same temperature as above for 16 hours. Subsequently, 0.20 ml (3.3 mmol) of 2-aminoethanol was added at room temperature and stirred at the same temperature as above for 30 minutes.

After the completion of the reaction, water was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure to obtain a concentration residue.

To a solution of 250 mg of the obtained concentration residue in 3 ml of ethanol, 25 mg of 20% palladium hydroxide/carbon (containing 50% water) was added in an argon atmosphere and after replacement with a hydrogen atmosphere under reduced pressure, stirred at room temperature for 2 hours.

After the completion of the reaction, replacement with an argon atmosphere was performed, and the reaction solution was filtered through celite. The solid on the celite was washed with ethanol, and all of the filtrates were concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=50:50 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 93 mg of the title compound (yield: 45% [3 steps]) as a white solid.

Mass spectrum (CI, m/z): 469 [M+1]⁺

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.19 & 11.83 (br s, total 1H), 9.84-9.47 (m, 1H), 7.27-7.21 (m, 4H), 7.18-7.12 (m, 1H), 4.72 (t, J=5.3 Hz, 1H), 4.57 (d, J=12.4 Hz, 1H), 4.44 (d, J=12.4 Hz, 1H), 3.60-3.52 (m, 2H), 3.27-3.19 (m, 1H), 2.75 (dd, J=6.0, 15.9 Hz, 1H), 2.58-2.52 (m, 1H), 2.48-2.40 (m, 2H), 2.25-2.12 (m, 2H), 1.89-1.72 (m, 2H), 1.61 (s, 3H), 1.49 (s, 3H), 0.08 (s, 9H).

Example 11 N-[5-(3-Hydroxy-3-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-562)

To a solution of 285 mg (0.543 mmol) of a mixture of ethyl 6,6-dimethyl-5-(3-oxo-3-phenylpropanoyl)-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylat e synthesized in the similar manner as in Reference Example 20 and (Z)-ethyl 5-(3-hydroxy-3-phenylacryloyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate as a tautomer in 5 ml of methanol, 9.2 mg (0.24 mmol) of sodium borohydride was added at 0° C. in a nitrogen atmosphere and stirred for 1.5 hours after the temperature was raised to room temperature.

After the completion of the reaction, 10 ml of a saturated aqueous solution of ammonium chloride and dichloromethane were added to the reaction solution and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with dichloromethane, all of the obtained organic layers were dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 98:2 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with dichloromethane/n-hexane, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 88 mg of the title compound (yield: 35%) as a white solid.

Mass spectrum (DUIS, m/z): 455 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.23 & 11.85 (br s, total 1H), 9.75-9.43 (m, 1H), 7.44-7.13 (m, 5H), 5.35 (d, J=4.1 Hz, 1H), 5.05-4.98 (m, 1H), 4.57 (d, J=11.7 Hz, 1H), 4.35 (d, J=11.7 Hz, 1H), 2.65 (dd, J=8.9, 15.1 Hz, 1H), 2.57-2.35 (m, 3H), 2.25-2.09 (m, 2H), 1.89-1.72 (m, 2H), 1.65 (s, 3H), 1.61 (s, 3H), 0.06 (s, 9H).

Example 12 (R)—N-(3-Hydroxy-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-227)

To a solution of 216 mg (0.489 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 4.5 ml of 1,4-dioxane, 379 mg (2.51 mmol) of (R)-3-amino-3-phenylpropan-1-ol [purchased from Ark Pharm, Inc.] and 0.17 ml (0.99 mmol) of DIPEA were added at room temperature in an argon atmosphere, then applied to a microwave reaction apparatus, and reacted at 100° C. for 1 hour. After standing to cool, 1.0 ml of methanol and 0.5 ml of triethylamine were added, applied to a microwave reaction apparatus, and reacted at 80° C. for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and ethyl acetate, water, and a saturated aqueous solution of sodium chloride were added thereto and then the aqueous layer and the organic layer were separated. The organic layer was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=99:1 to 96:4 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with ethyl acetate/diisopropyl ether, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 173 mg of the title compound (yield: 73%) as a white solid.

Mass spectrum (CI, m/z): 484 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.19 & 11.66 (s, total 1H), 9.61-9.47 (m, 1H), 7.39-7.13 (m, 5H), 6.46 & 6.38 (d, J=8.0 Hz, total 1H), 4.92-4.83 (m, 1H), 4.66-4.33 (m, 3H), 3.46-3.34 (m, 2H), 2.50-2.41 (m, 2H), 2.26-2.13 (m, 2H), 2.01-1.72 (m, 4H), 1.65-1.47 (m, 6H), 0.12-0.06 (m, 9H).

Example 13 (R)—N-(3-Hydroxy-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. III-226)

To a solution of 468 mg (1.17 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate hydrochloride synthesized in the similar manner as in Reference Example 7 in 10 ml of dehydrated dichloromethane, 0.72 ml (4.1 mmol) of DIPEA was added at room temperature in a nitrogen atmosphere, and then, 235 mg (0.791 mmol) of bis(trichloromethyl)carbonate was added at −78° C. and stirred at the same temperature as above for 3 hours.

After the completion of the reaction, 20 ml of a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred while the temperature was raised to room temperature for a while. The organic layer and the aqueous layer were separated, and then, the aqueous layer was subjected to extraction with dichloromethane twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 75:25 (V/V)), and a fraction containing ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate was concentrated under reduced pressure and dried under reduced pressure to obtain 490 mg of a concentration residue.

To a solution of 113 mg of the obtained concentration residue in 2 ml of dehydrated THF, 0.14 ml (0.80 mmol) of DIPEA and 105 mg (0.692 mmol) of (R)-3-amino-3-phenylpropan-1-ol [purchased from Ark Pharm, Inc.] were added at room temperature in a nitrogen atmosphere and then stirred for 2.5 hours while heated to reflux. Subsequently, 0.10 ml (1.7 mmol) of 2-aminoethanol was added and then stirred for 2 hours while heated to reflux.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. 0.1 ml of acetic acid was added to the obtained concentration residue and then subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=50:50 to 15:85 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel column chromatography (elution solvent: dichloromethane:methanol=99:1 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with ethyl acetate/n-hexane, and the deposited solid was collected by filtration, washed by sousing with n-hexane, and then dried under reduced pressure to obtain 49 mg of the title compound (yield: 39% [2 steps]) as a white solid.

Mass spectrum (CI, m/z): 470 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.22 & 11.84 (br s, total 1H), 9.91-9.66 (m, 1H), 7.37-7.26 (m, 4H), 7.21-7.14 (m, 1H), 6.50-6.28 (m, 1H), 4.92-4.80 (m, 1H), 4.65-4.52 (m, 1H), 4.49-4.31 (m, 2H), 3.44-3.36 (m, 2H), 2.00-1.77 (m, 2H), 1.59 (br s, 3H), 1.51 (br s, 3H), 1.06-0.93 (m, 2H), 0.81-0.61 (m, 2H), 0.03 (s, 9H).

Example 14 (R)—N-(4-Hydroxy-1-phenylbutyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-283)

To a solution of 100 mg (0.227 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 and 138 mg (0.684 mmol) of (R)-4-amino-4-phenylbutan-1-ol hydrochloride [purchased from NetChem, Inc.] in 2 ml of dehydrated 1,4-dioxane, 0.24 ml (1.4 mmol) of DIPEA was added at room temperature in an argon atmosphere and stirred at 100° C. for 3 hours. Subsequently, 1 ml of triethylamine and 1 ml of ethanol were added to the reaction solution and heated and stirred at 80° C. for 5 hours.

After the completion of the reaction, water was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, dried by adding anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=50:50 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 91.3 mg of the title compound (yield: 81%) as a white solid.

Mass spectrum (CI, m/z): 498 [M+1]⁺

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.18 & 11.73 (s, total 1H), 9.66-9.40 (m, 1H), 7.38-7.33 (m, 2H), 7.33-7.26 (m, 2H), 7.21-7.13 (m, 1H), 6.43-6.16 (m, 1H), 4.75-4.66 (m, 1H), 4.47 (br s, 2H), 4.38 (t, J=5.2 Hz, 1H), 3.45-3.35 (m, 2H), 2.49-2.42 (m, 2H), 2.25-2.14 (m, 2H), 1.88-1.64 (m, 4H), 1.60 (br s, 3H), 1.55-1.28 (m, 5H), 0.09 (s, 9H).

Example 15 (R)—N-(5-Hydroxy-1-phenylpentyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-291)

To a solution of 9.50 ml (9.50 mmol) of 1 M lithium aluminum hydride/THF solution in 40 ml of dehydrated THF, a solution of 2.02 g (6.28 mmol) of (R)-ethyl 5-[(tert-butoxycarbonyl)amino]-5-phenylpentanoate [synthesized according to the method described in Tetrahedron Lett., 1998, 39, 5951-5954] in 20 ml of dehydrated THF was added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, 50 ml of THF was added, and then, 0.4 ml of water and 1.6 ml (1.6 mmol) of a 1 N aqueous sodium hydroxide solution were added and stirred at the same temperature as above for 30 minutes. The deposited solid was filtered using a celite filter, and the solid was washed with ethyl acetate. The obtained filtrate was concentrated under reduced pressure and dried under reduced pressure to obtain a concentration residue.

To a solution of 1.68 g of the obtained concentration residue in 20 ml of dichloromethane, 2 ml of trifluoroacetic acid was added at room temperature in an argon atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure and dried under reduced pressure to obtain 1.35 g of a concentration residue.

To a solution of 905 mg of the obtained concentration residue in 3 ml of dehydrated THF, 0.60 ml (3.4 mmol) of DIPEA was added with stirring in an argon atmosphere, and then, 205 mg (0.465 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 was added at room temperature and stirred at 60° C. for 4 hours. Subsequently, 0.5 ml of triethylamine and 1 ml of methanol were added to the reaction solution, heated and stirred at 60° C. for 3 hours, and subsequently stirred at room temperature for 15 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (DIOL silica gel, elution solvent: dichloromethane:methanol=100:0 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure. The obtained concentration residue was further subjected to silica gel chromatography (DNH silica gel, elution solvent: dichloromethane:methanol=100:0 to 93:7 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=70:30 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 131 mg of the title compound (yield: 55%) as a white solid.

Mass spectrum (CI, m/z): 512 [M+1]⁺

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.18 & 11.64 (br s, total 1H), 9.58-9.47 (m, 1H), 7.38-7.33 (m, 2H), 7.32-7.25 (m, 2H), 7.21-7.14 (m, 1H), 6.38-6.15 (m, 1H), 4.75-4.65 (m, 1H), 4.52-4.38 (m, 2H), 4.33 (t, J=5.2 Hz, 1H), 3.39-3.33 (m, 2H), 2.49-2.42 (m, 2H), 2.26-2.14 (m, 2H), 1.88-1.72 (m, 3H), 1.72-1.30 (m, 10H), 1.27-1.14 (m, 1H), 0.13-0.06 (m, 9H).

Example 16 (S)—N-(2-Hydroxy-2-methyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-171)

To a solution of 200 mg (0.454 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 3 ml of dehydrated THF, 0.16 ml (0.92 mmol) of DIPEA and 385 mg (2.33 mmol) of (S)-1-amino-2-methyl-1-phenylpropan-2-ol [purchased from IS Chemical Technology Ltd.] were added at room temperature in an argon atmosphere and stirred at 60° C. for 4 hours. Subsequently, 1 ml of methanol and 1 ml of triethylamine were added at room temperature and stirred at the same temperature as above for 15 hours.

After the completion of the reaction, water was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, dried by adding anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (DIOL silica gel, elution solvent: dichloromethane:methanol=100:0 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure. The obtained concentration residue was subjected again to silica gel chromatography (DIOL silica gel, elution solvent: dichloromethane:methanol=100:0 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 182 mg of the title compound (yield: 81%) as a white solid.

Mass spectrum (DUIS, m/z): 498 [M+1]⁺

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.22 & 11.78 (br s, total 1H), 9.74-9.49 (m, 1H), 7.38-7.16 (m, 5H), 5.90-5.74 (m, 1H), 4.85 (s, 1H), 4.65-4.35 (m, 3H), 2.49-2.41 (m, 2H), 2.28-2.15 (m, 2H), 1.91-1.73 (m, 2H), 1.67-1.44 (m, 6H), 1.22 (s, 3H), 0.91 (s, 3H), 0.09 (s, 9H).

Example 17 (S)—N-(2-Hydroxy-2-methyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. III-170)

To a solution of 468 mg (1.17 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate hydrochloride synthesized in the similar manner as in Reference Example 7 in 10 ml of dehydrated dichloromethane, 0.72 ml (4.1 mmol) of DIPEA was added at room temperature in a nitrogen atmosphere, and then, 235 mg (0.791 mmol) of bis(trichloromethyl)carbonate was added at −78° C. and stirred at the same temperature as above for 3 hours.

After the completion of the reaction, 20 ml of a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred while the temperature was raised to room temperature for a while. The organic layer and the aqueous layer were separated, and then, the aqueous layer was subjected to extraction with dichloromethane twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 75:25 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 490 mg of a concentration residue.

To a solution of 112 mg of the obtained concentration residue in 2 ml of dehydrated THF, 0.14 ml (0.80 mmol) of DIPEA and 109 mg (0.660 mmol) of (S)-1-amino-2-methyl-1-phenylpropan-2-ol [purchased from IS Chemical Technology Ltd.] were added in this order at room temperature in a nitrogen atmosphere and then stirred for 3 hours while heated to reflux. Subsequently, 0.10 ml (1.7 mmol) of 2-aminoethanol was added and then stirred for 2.5 hours while heated to reflux.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. 0.1 ml of acetic acid was added to the obtained concentration residue and then subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=50:50 to 20:80 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with ethyl acetate/n-hexane, and the deposited solid was collected by filtration, washed by sousing with n-hexane, and then dried under reduced pressure to obtain 100 mg of the title compound (yield: 77% [2 steps]) as a white solid.

Mass spectrum (CI, m/z): 484 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.24 & 11.90 (br s, total 1H), 10.02-9.68 (m, 1H), 7.38-7.16 (m, 5H), 5.89-5.71 (m, 1H), 4.82 (s, 1H), 4.59 (d, J=8.4 Hz, 1H), 4.56-4.31 (m, 2H), 1.66-1.43 (m, 6H), 1.21 (s, 3H), 1.06-0.97 (m, 2H), 0.91 (s, 3H), 0.81-0.61 (m, 2H), 0.04 (s, 9H).

Example 18 N-(3-Hydroxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-354)

To a solution of 152 mg (0.346 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 and 201 mg (1.12 mmol) of 3-amino-2,2-dimethyl-3-phenylpropan-1-ol [synthesized according to the method described in Synthetic Communications 1994, 24 (7), 899-906] in 4 ml of 1,4-dioxane, 0.18 ml (1.0 mmol) of DIPEA was added at room temperature in an argon atmosphere, then applied to a microwave reaction apparatus, and reacted at 100° C. for 1 hour. After standing to cool, the reaction solution was concentrated under reduced pressure, and 4 ml of methanol and 1 ml of triethylamine were added to the obtained concentration residue and stirred at room temperature for 15 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, the obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: ethyl acetate:methanol=99:1 to 97:3 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=99:1 to 92:8 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with dichloromethane/n-hexane, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 55 mg of the title compound (yield: 31%) as a white solid.

Mass spectrum (DUIS, m/z): 512 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.95 (br s, total 1H), 9.89-9.36 (m, 1H), 7.36-7.17 (m, 5H), 6.85 (d, J=8.1 Hz, 1H), 5.50-5.39 (m, 1H), 4.64 (d, J=8.1 Hz, 1H), 4.47-4.28 (m, 2H), 3.30-3.22 (m, 1H), 3.03 (dd, J=4.1, 10.4 Hz, 1H), 2.49-2.40 (m, 2H), 2.28-2.13 (m, 2H), 1.92-1.71 (m, 2H), 1.60 (br s, 3H), 1.53 (s, 3H), 1.06 (s, 3H), 0.64 (s, 3H), 0.09 (s, 9H).

Example 19 (R)—N-(3-Hydroxy-3-methyl-1-phenylbutyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-299)

To a solution of 132 mg (0.300 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 and 155 mg (0.865 mmol) of (R)-4-amino-2-methyl-4-phenylbutan-2-ol synthesized in the similar manner as in Reference Example 23 in 4 ml of 1,4-dioxane, 0.15 ml (0.86 mmol) of DIPEA was added at room temperature in an argon atmosphere and then stirred at 100° C. for 2 hours. After standing to cool, the reaction solution was concentrated under reduced pressure, and 4 ml of methanol and 1 ml of triethylamine were added to the obtained concentration residue and stirred at room temperature for 18 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and ethyl acetate, water, and a saturated aqueous solution of sodium chloride were added to the obtained concentration residue and then the aqueous layer and the organic layer were separated. The obtained organic layer was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=98:2 to 91:9 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with dichloromethane/diethyl ether/n-hexane, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 104 mg of the title compound (yield: 68%) as a white solid.

Mass spectrum (DUIS, m/z): 512 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.73 (br s, 1H), 9.66-9.40 (m, 1H), 7.37-7.25 (m, 4H), 7.19-7.13 (m, 1H), 6.54 (d, J=5.3 Hz, 1H), 4.95-4.84 (m, 1H), 4.75-4.57 (m, 1H), 4.45 (br s, 2H), 2.47-2.42 (m, 2H), 2.25-2.14 (m, 2H), 2.02-1.74 (m, 3H), 1.65 (dd, J=3.3, 14.3 Hz, 1H), 1.58 (s, 3H), 1.53 (s, 3H), 1.16 (s, 3H), 1.13 (s, 3H), 0.09 (s, 9H).

Example 20 (S)—N-(2-Methoxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-123)

To a solution of 201 mg (0.456 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 4.5 ml of 1,4-dioxane, 0.16 ml (0.91 mmol) of DIPEA and 213 mg (1.41 mmol) of (S)-2-methoxy-1-phenylamine [synthesized according to the method described in J. Chem. Soc., Perkin Transactions 1, 2002, 20, 2237-2242] were added at room temperature, then applied to a microwave reaction apparatus, and reacted at 100° C. for 1 hour. Subsequently, 1 ml of methanol and 0.5 ml of triethylamine were added and then reacted at 80° C. for 1 hour in a microwave reaction apparatus again.

After the completion of the reaction, 8 ml of ethyl acetate, 0.4 ml of water, and 8 ml of a saturated aqueous solution of sodium chloride were added to the reaction solution and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with 10 ml of dichloromethane. All of the obtained organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. Diethyl ether was added to the obtained concentration residue and ultrasonicated, and then, the deposited insoluble matter was collected by filtration and dried under reduced pressure to obtain 180 mg of the title compound (yield: 82%) as a white solid.

Mass spectrum (CI, m/z): 484 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.67 (br s, total 1H), 9.68-9.41 (m, 1H), 7.41-7.35 (m, 2H), 7.34-7.27 (m, 2H), 7.25-7.17 (m, 1H), 6.44-6.13 (m, 1H), 5.02-4.92 (m, 1H), 4.57-4.39 (m, 2H), 3.63 (dd, J=7.9, 9.9 Hz, 1H), 3.50 (dd, J=6.0, 9.9 Hz, 1H), 3.26 (s, 3H), 2.49-2.42 (m, 2H), 2.26-2.15 (m, 2H), 1.92-1.73 (m, 2H), 1.60 (br s, 3H), 1.53 (br s, 3H), 0.09 (s, 9H).

Example 21 (S)—N-[2-(Difluoromethoxy)-1-phenylethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-131)

To a solution of 210 mg (0.697 mmol) of (S)-2-(difluoromethoxy)-1-phenylethanamine trifluoroacetate synthesized in the similar manner as in Reference Example 25 and 0.425 ml (2.43 mmol) of DIPEA in 3 ml of dehydrated 1,4-dioxane, 107 mg (0.243 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 was added at room temperature in an argon atmosphere and heated and stirred at 100° C. for 1 hour. Subsequently, 1 ml of triethylamine and 1 ml of methanol were added to the reaction solution and heated and stirred at 80° C. for 1 hour.

After the completion of the reaction, water was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, dried by adding anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=50:50 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 40.5 mg of the title compound (yield: 32%) as a white solid.

Mass spectrum (CI, m/z): 520 [M+1]⁺

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 (br s, 1H), 10.12-9.41 (m, 1H), 7.43-7.38 (m, 2H), 7.38-7.32 (m, 2H), 7.28-7.23 (m, 1H), 6.70 (t, J=76.0 Hz, 1H), 6.59-6.46 (m, 1H), 5.10-5.01 (m, 1H), 4.52-4.43 (m, 2H), 4.13 (dd, J=8.3, 10.4 Hz, 1H), 4.05-3.99 (m, 1H), 2.48-2.42 (m, 2H), 2.24-2.15 (m, 2H), 1.88-1.75 (m, 2H), 1.60 (s, 3H), 1.53 (s, 3H), 0.09 (s, 9H).

Example 22 (S)—N-(2-Ethoxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-139)

To a solution of 136 mg (0.308 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 and 162 mg (0.979 mmol) of (S)-2-ethoxy-1-phenylethanamine synthesized in the similar manner as in Reference Example 26 in 4 ml of 1,4-dioxane, 0.16 ml (0.92 mmol) of DIPEA was added at room temperature in an argon atmosphere and then stirred at 100° C. for 2 hours. After standing to cool, the reaction solution was concentrated under reduced pressure, and 4 ml of methanol and 1 ml of triethylamine were added to the obtained concentration residue, applied to a microwave reaction apparatus, and reacted at 80° C. for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, ethyl acetate was added to the obtained concentration residue, then the organic layer obtained by washing with a 10% aqueous potassium dihydrogen phosphate solution, a saturated aqueous solution of sodium bicarbonate, and a saturated aqueous solution of sodium chloride in this order was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=98:2 to 91:9 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with dichloromethane/diethyl ether/n-hexane, and the deposited solid was collected by filtration. The obtained solid was subjected again to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 93:7 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=100:0 to 67:33 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. Diethyl ether and n-hexane were added to the obtained concentration residue, and after ultrasonication, the deposited solid was collected by filtration and dried under reduced pressure to obtain 81 mg of the title compound (yield: 53%) as a white solid.

Mass spectrum (DUIS, m/z): 498 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.71 (br s, total 1H), 9.67-9.47 (m, 1H), 7.41-7.34 (m, 2H), 7.34-7.27 (m, 2H), 7.25-7.17 (m, 1H), 6.38-6.11 (m, 1H), 4.99-4.91 (m, 1H), 4.56-4.38 (m, 2H), 3.65 (dd, J=8.0, 9.9 Hz, 1H), 3.54 (dd, J=6.0, 9.9 Hz, 1H), 3.51-3.41 (m, 2H), 2.49-2.41 (m, 2H), 2.28-2.14 (m, 2H), 1.91-1.71 (m, 2H), 1.61 (br s, 3H), 1.54 (br s, 3H), 1.08 (t, J=7.0 Hz, 3H), 0.09 (s, 9H).

Example 23 (R)—N-(3-Methoxy-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-235)

To a solution of 138 mg (0.314 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 and 163 mg (0.987 mmol) of (R)-3-methoxy-1-phenylpropan-1-amine synthesized in the similar manner as in Reference Example 27 in 4 ml of 1,4-dioxane, 0.16 ml (0.92 mmol) of DIPEA was added at room temperature in an argon atmosphere and then stirred at 100° C. for 2 hours. After standing to cool, the reaction solution was concentrated under reduced pressure, and 4 ml of methanol and 1 ml of triethylamine were added to the obtained residue and stirred at room temperature for 18 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, ethyl acetate was added to the obtained concentration residue, then the organic layer obtained by washing with a 10% aqueous potassium dihydrogen phosphate solution, a saturated aqueous solution of sodium bicarbonate, and a saturated aqueous solution of sodium chloride in this order was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=95:5 to 88:12 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. Diethyl ether and n-hexane were added to the obtained concentration residue and ultrasonicated, and then, the deposited solid was collected by filtration and dried under reduced pressure to obtain 88 mg of the title compound (yield: 56%) as a white solid.

Mass spectrum (DUIS, m/z): 498 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.18 & 11.73 (br s, total 1H), 9.54 (br s, 1H), 7.35-7.28 (m, 4H), 7.22-7.16 (m, 1H), 6.41 (br s, 1H), 4.91-4.79 (m, 1H), 4.53-4.40 (m, 2H), 3.32-3.27 (m, 2H), 3.23 (s, 3H), 2.50-2.42 (m, 2H), 2.26-2.15 (m, 2H), 2.08-1.70 (m, 4H), 1.60 (s, 3H), 1.52 (s, 3H), 0.09 (s, 9H).

Example 24 Sodium (S)-2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylacetate (sodium salt of Compound No. IV-403)

To a solution of 98.0 mg (0.171 mmol) of (S)-benzyl 2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylacetate synthesized in the similar manner as in Example 55 in 15 ml of ethanol, 19.9 mg of palladium/carbon [ASCA2 (trade name), manufactured by N.E. Chemcat Corp., containing 52% water] was added in a nitrogen atmosphere and then, after replacement with a hydrogen atmosphere under reduced pressure, stirred at room temperature for 50 minutes.

After the completion of the reaction, replacement with an argon atmosphere was performed, and the reaction solution was filtered through celite. 14.8 mg (0.176 mmol) of sodium bicarbonate was added to the obtained filtrate and concentrated under reduced pressure. Purified water and diethyl ether were added to the obtained concentration residue and then dried under reduced pressure to obtain 82 mg of the title compound (yield: 95%) as a white solid.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.41 (br s, 1H), 9.95 (br. s, 1H), 7.38-7.30 (m, 2H), 7.24-7.17 (m, 2H), 7.14-7.08 (m, 1H), 6.42 (d, J=4.6 Hz, 1H), 4.68 (d, J=4.6 Hz, 1H), 4.48 (d, J=11.3 Hz, 1H), 4.45 (d, J=11.3 Hz, 1H), 2.51-2.41 (m, 2H), 2.28-2.14 (m, 2H), 1.90-1.74 (m, 2H), 1.59 (s, 3H), 1.55 (s, 3H), 0.08 (s, 9H).

Example 25 (R)—N-(2-Hydroxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-115)

To a solution of 127 mg (0.287 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 and 203 mg (1.48 mmol) of (R)-2-amino-2-phenylethanol in 3 ml of THF, 0.15 ml (0.86 mmol) of DIPEA was added at room temperature in an argon atmosphere and then stirred at 60° C. for 3 hours.

After the completion of the reaction, ethyl acetate, water, and a saturated aqueous solution of sodium chloride were added to the reaction solution and then the aqueous layer and the organic layer were separated. The obtained organic layer was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 98:2 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel column chromatography (elution solvent: ethyl acetate:a mixed solution of 28% aqueous ammonia solution/ethanol [1:5 (V/V)]=98:2 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 82 mg of the title compound (yield: 61%) as a white foam.

Mass spectrum (DUIS, m/z): 470 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.79 (br s, total 1H), 9.73-9.49 (m, 1H), 7.44-7.11 (m, 5H), 6.25-6.00 (m, 1H), 4.95-4.70 (m, 2H), 4.62-4.41 (m, 2H), 3.71-3.52 (m, 2H), 2.48-2.41 (m, 2H), 2.27-2.13 (m, 2H), 1.93-1.73 (m, 2H), 1.71-1.43 (m, 6H), 0.09 (br s, 9H).

Example 26 N-[1-(2-Fluorophenyl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-510)

To a solution of 201 mg (0.456 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 5 ml of 1,4-dioxane, 0.23 ml (1.4 mmol) of DIPEA and 212 mg (1.37 mmol) of 2-amino-2-(2-fluorophenyl)ethanol [purchased from Amatek Chemical Co., Ltd.] were added at room temperature in an argon atmosphere and then reacted at 100° C. for 1 hour. The reaction solution was concentrated under reduced pressure, and then, 4 ml of methanol and 1 ml of triethylamine were added to the concentration residue and reacted at 65° C. for 4.5 hours and further at 70° C. for 1.5 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and the obtained concentration residue was dissolved in 5 ml of ethyl acetate and washed with 10 ml of a 5% aqueous potassium bisulfate solution twice. All of the obtained organic layers were washed with 10 ml of a saturated aqueous solution of sodium bicarbonate, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 98:2 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 131 mg of the title compound (yield: 59%) as a white foam.

Mass spectrum (CI, m/z): 488 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.41-11.66 (m, 1H), 9.94-9.30 (m, 1H), 7.51-7.42 (m, 1H), 7.31-7.06 (m, 3H), 6.19 (br s, 1H), 5.15-5.04 (m, 1H), 4.98 (t, J=6.0 Hz, 1H), 4.54 (br s, 2H), 3.64-3.54 (m, 2H), 2.49-2.42 (m, 2H), 2.26-2.15 (m, 2H), 1.87-1.76 (m, 2H), 1.60 (s, 3H), 1.51 (s, 3H), 0.10 (s, 9H).

Example 27 (S)—N-[1-(3-Fluorophenyl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-519)

To a solution of 201 mg (0.456 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 5.0 ml of 1,4-dioxane, 0.23 ml (1.4 mmol) of DIPEA and 212 mg (1.37 mmol) of (S)-2-amino-2-(3-fluorophenyl)ethanol [purchased from Amatek Chemical Co., Ltd.] were added at room temperature in an argon atmosphere and then reacted at 100° C. for 1 hour. The reaction solution was concentrated under reduced pressure, and then, 4 ml of methanol and 1 ml of triethylamine were added to the concentration residue and reacted at room temperature for 17 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and the obtained concentration residue was dissolved in 5 ml of ethyl acetate, washed with 10 ml of a 5% aqueous potassium dihydrogen phosphate solution twice and 10 ml of a saturated aqueous solution of sodium bicarbonate once, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 98:2 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 128 mg of the title compound (yield: 58%) as a white foam.

Mass spectrum (CI, m/z): 488 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.35-11.70 (m, 1H), 9.84-9.41 (m, 1H), 7.38-7.29 (m, 1H), 7.21-7.15 (m, 2H), 7.05-6.98 (m, 1H), 6.21 (br s, 1H), 4.92 (t, J=5.8 Hz, 1H), 4.83-4.74 (m, 1H), 4.58-4.45 (m, 2H), 3.67-3.55 (m, 2H), 2.49-2.42 (m, 2H), 2.26-2.15 (m, 2H), 1.89-1.73 (m, 2H), 1.60 (s, 3H), 1.53 (s, 3H), 0.09 (s, 9H).

Example 28 (S)—N-[1-(4-Fluorophenyl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-527)

To a solution of 201 mg (0.456 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 5.0 ml of 1,4-dioxane, 0.23 ml (1.4 mmol) of DIPEA and 212 mg (1.37 mmol) of (S)-2-amino-2-(4-fluorophenyl)ethanol [purchased from Amatek Chemical Co., Ltd.] were added at room temperature in an argon atmosphere and then reacted at 100° C. for 1 hour. The reaction solution was concentrated under reduced pressure, and then, 4 ml of methanol and 1 ml of triethylamine were added to the concentration residue and reacted at room temperature for 15 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and the obtained concentration residue was dissolved in 5 ml of ethyl acetate, washed with 10 ml of a 5% aqueous potassium dihydrogen phosphate solution twice and 10 ml of a saturated aqueous solution of sodium bicarbonate once, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 98:2 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 98:2 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 139 mg of the title compound (yield: 63%) as a pale yellow foam.

Mass spectrum (CI, m/z): 488 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.71 (br s, total 1H), 9.75-9.43 (m, 1H), 7.42-7.33 (m, 2H), 7.15-7.06 (m, 2H), 6.28-6.02 (m, 1H), 4.89 (t, J=5.8 Hz, 1H), 4.81-4.72 (m, 1H), 4.51 (br s, 2H), 3.66-3.53 (m, 2H), 2.49-2.42 (m, 2H), 2.26-2.15 (m, 2H), 1.90-1.74 (m, 2H), 1.60 (br s, 3H), 1.53 (br s, 3H), 0.09 (s, 9H).

Example 29 N-[2-Hydroxy-1-(pyridin-2-yl)ethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-534)

To a solution of 152 mg (0.344 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 and 223 mg (1.06 mmol) of 2-amino-2-(pyridin-2-yl)ethanol dihydrochloride [purchased from J&W PharmLab, LLC] in 4 ml of 1,4-dioxane, 0.60 ml (3.4 mmol) of DIPEA was added at room temperature in an argon atmosphere, then applied to a microwave reaction apparatus, and reacted at 100° C. for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and a saturated aqueous solution of sodium bicarbonate was added to the concentration residue, followed by extraction with dichloromethane. The obtained organic layer was dried over anhydrous sodium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (DNH silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 93:7 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained residue was subjected again to silica gel column chromatography (DIOL silica gel, elution solvent: ethyl acetate:methanol=100:0 to 78:22 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 78 mg of the title compound (yield: 48%) as a white foam.

Mass spectrum (DUIS, m/z): 469 [M−1]⁻.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.22 & 11.78 (br s, total 1H), 9.79-9.45 (m, 1H), 8.54-8.49 (m, 1H), 7.74 (dt, J=1.7, 7.7 Hz, 1H), 7.42-7.36 (m, 1H), 7.28-7.21 (m, 1H), 6.19-6.00 (m, 1H), 4.92-4.82 (m, 2H), 4.62-4.43 (m, 2H), 3.76-3.65 (m, 2H), 2.49-2.42 (m, 2H), 2.27-2.15 (m, 2H), 1.92-1.72 (m, 2H), 1.68-1.50 (m, 6H), 0.10 (s, 9H).

Example 30 N-[2-Hydroxy-1-(pyridin-3-yl)ethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-542)

To a solution of 150 mg (0.341 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 and 218 mg (1.03 mmol) of 2-amino-2-(pyridin-3-yl)ethanol dihydrochloride [purchased from J&W PharmLab, LLC] in 4 ml of 1,4-dioxane, 0.60 ml (3.4 mmol) of DIPEA was added at room temperature in an argon atmosphere and then stirred at 100° C. for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and a saturated aqueous solution of sodium bicarbonate was added to the concentration residue, followed by extraction with dichloromethane. The obtained organic layer was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. 4 ml of methanol and 1 ml of triethylamine were added to the obtained concentration residue, applied to a microwave reaction apparatus, and reacted at 80° C. for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, the obtained concentration residue was subjected to silica gel column chromatography (DNH silica gel, elution solvent: 1,2-dichloroethane:methanol=95:5 to 88:12 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained residue was subjected again to silica gel column chromatography (DNH silica gel, elution solvent: ethyl acetate:methanol=96:4 to 70:30 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained residue was subjected again to silica gel column chromatography (DIOL silica gel, elution solvent: ethyl acetate:methanol=99:1 to 73:27 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 27 mg of the title compound (yield: 17%) as a white foam.

Mass spectrum (DUIS, m/z): 471 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.77 (br s, total 1H), 9.75-9.47 (m, 1H), 8.54 (d, J=2.0 Hz, 1H), 8.41 (dd, J=2.0, 4.7 Hz, 1H), 7.75 (ddd, J=2.0, 2.0, 7.6 Hz, 1H), 7.32 (dd, J=4.7, 7.6 Hz, 1H), 6.39-6.13 (m, 1H), 4.97 (t, J=5.8 Hz, 1H), 4.84-4.76 (m, 1H), 4.61-4.42 (m, 2H), 3.71-3.59 (m, 2H), 2.49-2.42 (m, 2H), 2.27-2.14 (m, 2H), 1.89-1.72 (m, 2H), 1.60 (br s, 3H), 1.52 (br s, 3H), 0.09 (s, 9H).

Example 31 N-[1-(Benzo[d][1,3]dioxol-4-yl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-502)

To a solution of 240 mg (0.815 mmol) of 1-(benzo[d][1,3]dioxol-4-yl)-2-[(tert-butyldimethylsilyl)oxy]ethanamin e synthesized in the similar manner as in Reference Example 32 in 10 ml of dichloromethane, 1 ml (4 mmol) of 4 N hydrogen chloride/1,4-dioxane solution was added at room temperature and stirred at room temperature for 2 hours. The reaction solution was concentrated under reduced pressure, and 3 ml of THF, 0.210 ml (1.24 mmol) of DIPEA, and 93.0 mg (0.211 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 were added to the obtained residue at room temperature and stirred at 60° C. for 8 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and ethyl acetate, a saturated aqueous solution of sodium chloride, and water were added thereto and then the aqueous layer and the organic layer were separated. The obtained organic layer was dried over anhydrous magnesium sulfate, filtered, and then concentrated under reduced pressure. 2 ml of methanol and 2 ml of triethylamine were added to the obtained concentration residue, applied to a microwave reaction apparatus, and reacted at 80° C. for 30 minutes.

After the completion of the reaction, the concentration residue obtained by concentration under reduced pressure was subjected to silica gel column chromatography (elution solvent: ethyl acetate:a mixed solution of 28% aqueous ammonia solution/ethanol [1:5 (V/V)]=98:2 to 95:5 (V/V)), and a fraction containing N-{1-(benzo[d][1,3]dioxol-4-yl)-2-[(tert-butyldimethylsilyl)oxy]ethyl}-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 119 mg (0.190 mmol) of the obtained concentration residue in 3.5 ml of dehydrated dichloromethane, 0.18 ml (1.0 mmol) of trimethylsilyl trifluoromethanesulfonate was added at 0° C. and stirred at the same temperature as above for 5 minutes, and then, 0.17 ml (1.5 mmol) of 2,6-lutidine and 0.18 ml (1.0 mmol) of trimethylsilyl trifluoromethanesulfonate were added at 0° C. and stirred at the same temperature as above for 5 minutes. Subsequently, 1 ml of methanol and 0.17 ml (1.5 mmol) of 2,6-lutidine were added, and then, the reaction solution was concentrated under reduced pressure. To a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane, 0.18 ml (1.0 mmol) of trimethylsilyl trifluoromethanesulfonate was added at 0° C. and stirred at the same temperature as above for 5 minutes, and then, 1.0 ml of dehydrated acetonitrile was added at 0° C. and stirred at the same temperature as above for 10 minutes.

After the completion of the reaction, 1 ml of methanol and 0.17 ml (1.5 mmol) of 2,6-lutidine were added to the reaction solution and then concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: ethyl acetate:a mixed solution of 28% aqueous ammonia solution/ethanol [1:5 (V/V)]=98:2 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel column chromatography (DIOL silica gel, elution solvent: ethyl acetate:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 52 mg of the title compound (yield: 48%) as a white solid.

Mass spectrum (DUIS, m/z): 514 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.72 (br s, total 1H), 9.69-9.50 (m, 1H), 6.89-6.83 (m, 1H), 6.81-6.76 (m, 2H), 6.12-5.94 (m, 3H), 4.96-4.90 (m, 2H), 4.59-4.43 (m, 2H), 3.62-3.56 (m, 2H), 2.49-2.42 (m, 2H), 2.26-2.15 (m, 2H), 1.90-1.74 (m, 2H), 1.60 (br s, 3H), 1.54 (br s, 3H), 0.10 (s, 9H).

Example 32 (S)—N-(1-Cyclohexyl-2-hydroxyethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-495)

To a solution of 326 mg (0.739 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 4 ml of dehydrated THF, 0.33 ml (1.9 mmol) of DIPEA and 304 mg (2.12 mmol) of (S)-2-amino-2-cyclohexylethanol [synthesized according to the method described in Bioorg. Med. Chem. Lett., 2009, 19, 926-929] were added at room temperature in a nitrogen atmosphere and then stirred for 1.5 hours while heated to reflux. Subsequently, 0.90 ml (6.5 mmol) of triethylamine and 0.90 ml (22 mmol) of methanol were added to the reaction solution and then stirred for 1.5 hours while heated to reflux.

After the completion of the reaction, water was added to the reaction solution, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. 85 μl of acetic acid was added to the obtained concentration residue and then subjected to silica gel column chromatography (DIOL silica gel, elution solvent: dichloromethane:methanol=100:0 to 97:3 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with dichloromethane/n-hexane, and the deposited solid was collected by filtration, washed by sousing with n-hexane, and then dried under reduced pressure to obtain 295 mg of the title compound (yield: 84%) as a white solid.

Mass spectrum (CI, m/z): 476 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.71 (br s, total 1H), 9.70-9.44 (m, 1H), 5.46-5.15 (m, 1H), 4.54 (t, J=5.0 Hz, 1H), 4.49-4.21 (m, 2H), 3.53-3.40 (m, 3H), 2.48-2.40 (m, 2H), 2.27-2.10 (m, 2H), 1.88-1.45 (m, 14H), 1.28-1.03 (m, 3H), 1.03-0.83 (m, 2H), 0.08 (s, 9H).

Example 33 (S)—N-(1-Hydroxy-3-methylbutan-2-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-475)

To a solution of 201 mg (0.456 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 4.5 ml of 1,4-dioxane, 235 mg (2.27 mmol) of (S)-2-amino-3-methylbutan-1-ol and 0.16 ml (0.91 mmol) of DIPEA were added at room temperature in a nitrogen atmosphere and then stirred at 100° C. for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and ethyl acetate, water, and a saturated aqueous solution of sodium chloride were added to the concentration residue and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with ethyl acetate, all of the obtained organic layers were dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=99:1 to 96:4 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. Acetone was added to the obtained concentration residue and then ultrasonicated, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 129 mg of the title compound (yield: 65%) as a white solid.

Mass spectrum (CI, m/z): 436 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.67 (br s, total 1H), 9.60-9.48 (m, 1H), 5.45-5.20 (m, 1H), 4.62-4.24 (m, 3H), 3.52-3.39 (m, 3H), 2.49-2.41 (m, 2H), 2.24-2.13 (m, 2H), 1.91-1.73 (m, 3H), 1.60 (br s, 6H), 0.92-0.82 (m, 6H), 0.08 (s, 9H).

Example 34 (S)—N-(1-Hydroxypropan-2-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-455)

To a solution of 200 mg (0.454 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 4.5 ml of 1,4-dioxane, 170 mg (2.26 mmol) of (S)-2-aminopropan-1-ol and 0.16 ml (0.91 mmol) of DIPEA were added at room temperature, then applied to a microwave reaction apparatus, and reacted at 100° C. for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and ethyl acetate, water, and a saturated aqueous solution of sodium chloride were added to the concentration residue and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with ethyl acetate, all of the obtained organic layers were dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=99:1 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. Ethyl acetate was added to the obtained concentration residue and ultrasonicated, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 145 mg of the title compound (yield: 78%) as a white solid.

Mass spectrum (CI, m/z): 408 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.18 & 11.64 (br s, total 1H), 9.52 (s, 1H), 5.70-5.32 (m, 1H), 4.65 (t, J=5.6 Hz, 1H), 4.44-4.28 (m, 2H), 3.77-3.64 (m, 1H), 3.41-3.34 (m, 1H), 3.30-3.23 (m, 1H), 2.49-2.40 (m, 2H), 2.24-2.13 (m, 2H), 1.88-1.72 (m, 2H), 1.60 (s, 6H), 1.05 (d, J=6.7 Hz, 3H), 0.08 (s, 9H).

Example 35 N-(2-Hydroxyethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-438)

To a solution of 200 mg (0.454 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 3 ml of dehydrated THF, 0.16 ml (0.92 mmol) of DIPEA and 0.14 ml (2.3 mmol) of 2-aminoethanol were added at room temperature in an argon atmosphere and stirred at 60° C. for 3 hours.

After the completion of the reaction, water was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried by adding anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=90:10 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 135 mg of the title compound (yield: 76%) as a white solid.

Mass spectrum (DUIS, m/z): 394 [M+1]⁺

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.19 & 11.60 (br s, total 1H), 9.54 (s, 1H), 6.05-5.85 (m, 1H), 4.66 (t, J=5.5 Hz, 1H), 4.42-4.28 (m, 2H), 3.45-3.36 (m 2H), 3.17-3.02 (m, 2H), 2.48-2.39 (m, 2H), 2.25-2.12 (m, 2H), 1.91-1.71 (m, 2H), 1.67-1.52 (m, 6H), 0.08 (s, 9H).

Example 36 N-(2-Hydroxy-2-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-450)

To a solution of 100 mg (0.227 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 2 ml of dehydrated 1,4-dioxane, 0.20 ml (1.1 mmol) of DIPEA and 160 mg (1.17 mmol) of 2-amino-1-phenylethanol were added at room temperature in an argon atmosphere and stirred at the same temperature as above for 1 hour.

After the completion of the reaction, water was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried by adding anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=50:50 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 82.0 mg of the title compound (yield: 77%) as a white solid.

Mass spectrum (CI, m/z): 470 [M+1]⁺

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.38-11.74 (m, 1H), 9.59 (br s, 1H), 7.36-7.29 (m, 4H), 7.26-7.20 (m, 1H), 6.14-5.98 (m, 1H), 5.58 (d, J=4.0 Hz, 1H), 4.70-4.62 (m, 1H), 4.42-4.28 (m, 2H), 3.29-3.23 (m, 1H), 3.10 (ddd, J=4.8, 8.0, 13.2 Hz, 1H), 2.48-2.40 (m, 2H), 2.23-2.14 (m, 2H), 1.88-1.74 (m, 2H), 1.60 (s, 6H), 0.08 (s, 9H).

Example 37 N-(2-Hydroxypropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-442)

To a solution of 100 mg (0.227 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 and 85 μl (1.1 mmol) of 1-amino-2-propanol in 2 ml of dehydrated 1,4-dioxane, 0.20 ml (1.1 mmol) of DIPEA was added at room temperature in an argon atmosphere and stirred at the same temperature as above for 1.5 hours.

After the completion of the reaction, water was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried by adding anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=50:50 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 61.1 mg of the title compound (yield: 66%) as a white solid.

Mass spectrum (CI, m/z): 408 [M+1]⁺

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.19 & 11.78 (br s, total 1H), 9.71-9.46 (m, 1H), 6.05-5.78 (m, 1H), 4.76 (d, J=4.4 Hz, 1H), 4.38 (br s, 2H), 3.71-3.61 (m, 1H), 3.09-2.99 (m, 1H), 2.97-2.88 (m, 1H), 2.49-2.39 (m, 2H), 2.25-2.13 (m, 2H), 1.88-1.71 (m, 2H), 1.60 (br s, 6H), 1.01 (d, J=6.3 Hz, 3H), 0.08 (s, 9H).

Example 38 N-[(2S)-1-Hydroxy-3-methyl-1-phenylbutan-2-yl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-487)

To a solution of 1.25 g (6.21 mmol) of (S)-tert-butyl (3-methyl-1-oxobutan-2-yl)carbamate [synthesized according to the method described in J. Am. Chem. Soc., 2004, 126, 11440-11441] in 15 ml of dehydrated THF, 6.60 ml (6.60 mmol) of 1 M phenyl magnesium bromide/THF solution was added dropwise at an internal temperature of 15° C. or lower in an argon atmosphere and, after the completion of the dropwise addition, stirred at room temperature for 1.5 hours.

After the completion of the reaction, the reaction solution was cooled in ice water, and 20 ml of a saturated aqueous solution of ammonium chloride was added and stirred at room temperature. Ethyl acetate and a saturated aqueous solution of sodium chloride were further added thereto and then the aqueous layer and the organic layer were separated. The obtained organic layer was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 70:30 (V/V)), and a fraction containing tert-butyl [(2 S)-1-hydroxy-3-methyl-1-phenylbutan-2-yl]carbamate was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 0.90 g of the obtained concentration residue in 10 ml of dichloromethane, 1.2 ml (10 mmol) of 2,6-lutidine and 1.8 ml (10 mmol) of trimethylsilyl trifluoromethanesulfonate were added dropwise at 0° C. in a nitrogen atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, 50 ml of a saturated aqueous solution of sodium bicarbonate was added thereto, stirred, and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with dichloromethane, all of the obtained organic layers were dried over anhydrous sodium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The operation of adding toluene to the obtained concentration residue and concentrating the resultant under reduced pressure was repeated several times. The obtained concentration residue was subjected to silica gel column chromatography (DNH silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing (2S)-2-amino-3-methyl-1-phenylbutan-1-ol was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing (2 S)-2-amino-3-methyl-1-phenylbutan-1-ol was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 111 mg (0.251 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 4.0 ml of 1,4-dioxane, 97 mg of the concentration residue of (2S)-2-amino-3-methyl-1-phenylbutan-1-ol described above and 0.11 ml (0.63 mmol) of DIPEA were added at room temperature, then applied to a microwave reaction apparatus, and reacted at 100° C. for 1 hour. After the reaction, the reaction solution was concentrated under reduced pressure, and 4 ml of methanol and 1 ml of triethylamine were added to the obtained concentration residue, applied to a microwave reaction apparatus, and reacted at 80° C. for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, the obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. Diethyl ether and n-hexane were added to the obtained concentration residue and ultrasonicated, and the deposited solid was collected by filtration. The obtained solid was subjected again to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with acetone/n-heptane, and the deposited solid was collected by filtration. The obtained solid was subjected again to silica gel column chromatography (elution solvent: hexane:ethyl acetate=38:62 to 17:83 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. n-Hexane was added to the obtained concentration residue, and after ultrasonication, the deposited solid was collected by filtration and dried under reduced pressure to obtain 55 mg of the title compound (yield: 42%) as a white solid.

Mass spectrum (CI, m/z): 512 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.15 & 11.74 (br s, total 1H), 9.85-9.20 (m, 1H), 7.33-7.19 (m, 4H), 7.17-7.10 (m, 1H), 5.68 (d, J=5.8 Hz, 1H), 5.32-5.16 (m, 1H), 4.82 (dd, J=2.6, 5.8 Hz, 1H), 4.37-4.23 (m, 2H), 3.52 (ddd, J=2.6, 8.7, 8.7 Hz, 1H), 2.49-2.39 (m, 2H), 2.26-2.13 (m, 2H), 2.00-1.72 (m, 3H), 1.52 (br s, 3H), 1.31 (br s, 3H), 1.03 (d, J=6.7 Hz, 3H), 0.90 (d, J=6.7 Hz, 3H), 0.09 (s, 9H).

Example 39 N-(4-Hydroxy-1-phenyl-2-butyn-1-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-378)

To a solution of 106 mg (0.240 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 3 ml of dehydrated 1,4-dioxane, 0.24 ml (1.4 mmol) of DIPEA and 146 mg (0.739 mmol) of 4-amino-4-phenyl-2-butyn-1-ol hydrochloride synthesized in the similar manner as in Reference Example 33 were added in an argon atmosphere and stirred at 100° C. for 2 hours. Subsequently, 1 ml of triethylamine and 1 ml of methanol were added to the reaction solution and stirred at 80° C. for 1 hour.

After the completion of the reaction, water was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (DIOL column, elution solvent: dichloromethane:methanol=100:0 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel chromatography (elution solvent: dichloromethane:methanol=100:0 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 79.6 mg of the title compound (yield: 67%) as a light brown solid.

Mass spectrum (CI, m/z): 494 [M+1]⁺

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.70 (br s, total 1H), 9.54 (br s, 1H), 7.53-7.47 (m, 2H), 7.38-7.32 (m, 2H), 7.29-7.23 (m, 1H), 7.20-6.97 (m, 1H), 5.89-5.84 (m, 1H), 5.20 (t, J=5.9 Hz, 1H), 4.45 (br s, 2H), 4.15 (dd, J=1.9, 5.9 Hz, 2H), 2.48-2.40 (m, 2H), 2.24-2.12 (m, 2H), 1.87-1.73 (m, 2H), 1.63 (s, 3H), 1.59 (s, 3H), 0.08 (s, 9H).

Example 40 (S)-2-{6,6-Dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl acetate (Compound No. V-1442)

To a solution of 360 mg (0.816 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 10 ml of THF, 883 mg (4.09 mmol) of (S)-2-amino-2-phenylethyl acetate hydrochloride synthesized in the similar manner as in Reference Example 35 and 2.0 ml (12 mmol) of DIPEA were added at room temperature, applied to a microwave reaction apparatus, and reacted at 100° C. for 2 hours. Subsequently, 1.1 ml (27 mmol) of methanol was added, then applied to a microwave reaction apparatus, and reacted at 80° C. for 1 hour. 2.0 ml (49 mmol) of methanol and 1.0 ml (7.2 mmol) of triethylamine were further added, then applied to a microwave reaction apparatus, and reacted at 80° C. for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and 15 ml of ethyl acetate and 15 ml of a saturated aqueous solution of sodium chloride were added to the obtained concentration residue and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with 15 ml of dichloromethane. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. Ethyl acetate and diethyl ether were added in small amounts to the obtained concentration residue, then ultrasonicated, cooled in ice water, and then filtered. The obtained solid was subjected again to silica gel column chromatography (DIOL silica gel, elution solvent: ethyl acetate:methanol=100:0 to 99:1 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. Ethyl acetate and diethyl ether were added in small amounts to the obtained concentration residue, then ultrasonicated, cooled in ice water, and then filtered to obtain white solid A. The filtrate was concentrated under reduced pressure, the obtained concentration residue was subjected to silica gel column chromatography (elution solvent: ethyl acetate:methanol=100:0 to 99:1 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. Ethyl acetate and diethyl ether were added in small amounts to the obtained concentration residue, then ultrasonicated, cooled in ice water, and then filtered to obtain white solid B. The white solids A and B were dissolved in ethyl acetate, then diethyl ether was added, and the deposited solid was filtered and dried under reduced pressure to obtain 142 mg of the title compound (yield: 34%) as a white solid.

Mass spectrum (DUIS, m/z): 512 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.71 (br s, total 1H), 9.76-9.33 (m, 1H), 7.43-7.37 (m, 2H), 7.37-7.31 (m, 2H), 7.28-7.22 (m, 1H), 6.65-6.38 (m, 1H), 5.12-5.03 (m, 1H), 4.49 (br s, 2H), 4.30-4.19 (m, 2H), 2.49-2.41 (m, 2H), 2.25-2.14 (m, 2H), 1.98 (s, 3H), 1.89-1.74 (m, 2H), 1.61 (br s, 3H), 1.53 (br s, 3H), 0.09 (s, 9H).

Example 41 (S)-2-{6,6-Dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl propionate (Compound No. V-1446)

To a solution of 200 mg (0.369 mmol) of (S)-ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 38 and 0.10 ml (0.74 mmol) of triethylamine in 3 ml of dehydrated dichloromethane, 0.071 ml (0.55 mmol) of propionic anhydride and 9.7 mg (0.079 mmol) of 4-dimethylaminopyridine were added in this order at room temperature in an argon atmosphere and then reacted at room temperature for 5 hours. Subsequently, 1 ml of methanol and 0.5 ml of triethylamine were added and reacted at room temperature for 2 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and 10 ml of ethyl acetate, 0.5 ml of water, and 10 ml of a saturated aqueous solution of sodium chloride were added to the obtained concentration residue, and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with 10 ml of dichloromethane twice, and all of the obtained organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. Diethyl ether was added to the obtained concentration residue, and after ultrasonication, insoluble matter was filtered and dried under reduced pressure to obtain 138 mg of the title compound (yield: 71%) as a white solid.

Mass spectrum (CI, m/z): 526 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.66 (br s, total 1H), 9.70-9.39 (m, 1H), 7.45-7.30 (m, 4H), 7.28-7.21 (m, 1H), 6.64-6.39 (m, 1H), 5.16-5.03 (m, 1H), 4.57-4.39 (m, 2H), 4.32-4.19 (m, 2H), 2.49-2.41 (m, 2H), 2.27 (q, J=7.5 Hz, 2H), 2.24-2.14 (m, 2H), 1.91-1.72 (m, 2H), 1.67-1.47 (m, 6H), 0.99 (t, J=7.5 Hz, 3H), 0.09 (s, 9H).

Example 42 (S)-2-{6,6-Dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl butanoate (Compound No. V-1450)

To a solution of 250 mg (0.461 mmol) of a mixture of (S)-ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate synthesized in the similar manner as in Reference Example 38 and (S)-ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate and 0.10 ml (0.74 mmol) of triethylamine in 4.5 ml of 1,4-dioxane, 0.09 ml (0.6 mmol) of butyric anhydride and 9.0 mg (0.074 mmol) of 4-dimethylaminopyridine were added in this order at room temperature in an argon atmosphere and then reacted at 100° C. for 1.5 hours. Subsequently, 1.5 ml (37 mmol) of methanol and 0.75 ml (5.4 mmol) of triethylamine were added, applied to a microwave reaction apparatus, and reacted at 80° C. for 2 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and 8 ml of ethyl acetate, 0.4 ml of water, and 8 ml of a saturated aqueous solution of sodium chloride were added to the obtained concentration residue, and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with 10 ml of dichloromethane twice, and all of the obtained organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, then the obtained concentration residue was subjected again to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=100:0 to 51:49 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. Water was added to the concentration residue, and after ultrasonication, insoluble matter was filtered and dried under reduced pressure to obtain 80 mg of the title compound (yield: 32%) as a white solid.

Mass spectrum (CI, m/z): 540 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.65 (br s, total 1H), 9.69-9.40 (m, 1H), 7.45-7.37 (m, 2H), 7.37-7.29 (m, 2H), 7.28-7.21 (m, 1H), 6.64-6.39 (m, 1H), 5.15-5.04 (m, 1H), 4.57-4.38 (m, 2H), 4.31-4.20 (m, 2H), 2.49-2.41 (m, 2H), 2.28-2.14 (m, 4H), 1.92-1.73 (m, 2H), 1.64-1.44 (m, 8H), 0.83 (t, J=7.4 Hz, 3H), 0.09 (s, 9H).

Example 43 (S)-2-{6,6-Dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl pentanoate (Compound No. V-1458)

To a solution of 200 mg (0.369 mmol) of (S)-ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 38 and 0.10 ml (0.74 mmol) of triethylamine in 3 ml of 1,4-dioxane, 0.09 ml (0.5 mmol) of valeric anhydride and 9.0 mg (0.074 mmol) of 4-dimethylaminopyridine were added at room temperature in an argon atmosphere and then reacted at 100° C. for 1 hour. Subsequently, 1 ml of methanol and 0.5 ml of triethylamine were added, applied to a microwave reaction apparatus, and reacted at 80° C. for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and 10 ml of ethyl acetate and 10 ml of 10% potassium dihydrogen phosphate were added to the obtained concentration residue, and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with 10 ml of dichloromethane twice, and all of the obtained organic layers were washed with 10 ml of water, 10 ml of a saturated aqueous solution of sodium bicarbonate, and 10 ml of a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=100:0 to 51:49 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. Purified water was added to the obtained concentration residue, and after ultrasonication, insoluble matter was filtered and dried under reduced pressure to obtain 39 mg of the title compound (yield: 19%) as a white solid.

Mass spectrum (CI, m/z): 554 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.63 (br s, total 1H), 9.54 (s, 1H), 7.44-7.37 (m, 2H), 7.36-7.30 (m, 2H), 7.28-7.21 (m, 1H), 6.66-6.39 (m, 1H), 5.14-5.04 (m, 1H), 4.59-4.40 (m, 2H), 4.25 (d, J=7.5 Hz, 2H), 2.49-2.41 (m, 2H), 2.29-2.14 (m, 4H), 1.92-1.73 (m, 2H), 1.61 (br s, 3H), 1.56-1.41 (m, 5H), 1.29-1.18 (m, 2H), 0.80 (t, J=7.3 Hz, 3H), 0.09 (s, 9H).

Example 44 (S)-2-{6,6-Dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl octanoate (Compound No. V-1470)

To a solution of 183 mg (0.329 mmol) of a mixture of (S)-ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate synthesized in the similar manner as in Reference Example 38 and (S)-ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate in a 3 ml of dehydrated dichloromethane, 0.10 ml (0.72 mmol) of triethylamine, 0.15 ml (0.51 mmol) of n-octanoic anhydride, and 10.6 mg (0.087 mmol) of 4-dimethylaminopyridine were added in this order at room temperature in a nitrogen atmosphere and then stirred at the same temperature as above for 2 hours. Subsequently, 1.0 ml (7.2 mmol) of triethylamine and 1.0 ml (25 mmol) of methanol were added to the reaction solution and then stirred at room temperature for 20.5 hours. 1.0 ml (7.2 mmol) of triethylamine and 1.0 ml (25 mmol) of methanol were added to the reaction solution, stirred at 50° C. for 2 hours, and then stirred for 4 hours after the temperature was raised to 60° C.

After the completion of the reaction, water was added to the reaction solution, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: dichloromethane:methanol=100:0 to 97:3 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. n-Hexane was added to the obtained concentration residue, and after ultrasonication, the deposited solid was collected by filtration, washed by sousing with n-hexane, and then dried under reduced pressure to obtain 115 mg of the title compound (yield: 58%) as a white solid.

Mass spectrum (CI, m/z): 596 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.16 & 11.77 (br s, total 1H), 9.55 (br s, 1H), 7.47-7.37 (m, 2H), 7.37-7.29 (m, 2H), 7.29-7.20 (m, 1H), 6.64-6.43 (m, 1H), 5.16-5.02 (m, 1H), 4.49 (s, 2H), 4.34-4.18 (m, 2H), 2.49-2.41 (m, 2H), 2.28-2.14 (m, 4H), 1.89-1.73 (m, 2H), 1.60 (s, 3H), 1.53 (s, 3H), 1.50-1.43 (m, 2H), 1.24-1.13 (m, 8H), 0.83-0.75 (m, 3H), 0.09 (s, 9H).

Example 45 (S)-2-{6,6-Dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl dodecanoate (Compound No. V-1474)

To a solution of 202 mg (0.373 mmol) of (S)-ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 38, 0.11 ml (0.79 mmol) of triethylamine, and 10 mg (0.082 mmol) of 4-dimethylaminopyridine in 2 ml of dehydrated dichloromethane, 224 mg (0.585 mmol) of dodecanoic anhydride was added at room temperature in an argon atmosphere and stirred at room temperature for 1 hour. Subsequently, 1 ml of triethylamine and 1 ml of methanol were added to the reaction solution and stirred at room temperature for 16 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=95:5 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 139 mg of the title compound (yield: 57%) as a white solid.

Mass spectrum (CI, m/z): 652 [M+1]⁺

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.18 & 11.66 (br s, total 1H), 9.83-9.28 (m, 1H), 7.42-7.37 (m, 2H), 7.37-7.30 (m, 2H), 7.28-7.21 (m, 1H), 6.67-6.35 (m, 1H), 5.14-5.03 (m, 1H), 4.56-4.42 (m, 2H), 4.30-4.20 (m, 2H), 2.49-2.42 (m, 2H), 2.28-2.13 (m, 4H), 1.89-1.73 (m, 2H), 1.60 (br s, 3H), 1.57-1.43 (m, 5H), 1.30-1.14 (m, 16H), 0.85 (t, J=6.9 Hz, 3H), 0.09 (s, 9H).

Example 46 (S)-2-{6,6-Dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl palmitate (Compound No. V-1478)

To a solution of 220 mg (0.406 mmol) of (S)-ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 38, 0.115 ml (0.825 mmol) of triethylamine, and 300 mg (0.606 mmol) of palmitic anhydride in 3 ml of dichloromethane, 10 mg (0.082 mmol) of 4-dimethylaminopyridine was added at room temperature in an argon atmosphere and stirred at the same temperature as above for 1.5 hours. Subsequently, 1.0 ml of methanol and 0.5 ml of triethylamine were added to the reaction solution and stirred at room temperature for 15 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 195 mg of the title compound (yield: 68%) as a white solid.

Mass spectrum (DUIS, m/z): 708 [M+1]⁺

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.18 & 11.64 (br s, total 1H), 9.64-9.50 (m, 1H), 7.43-7.38 (m, 2H), 7.36-7.30 (m, 2H), 7.27-7.21 (m, 1H), 6.63-6.39 (m, 1H), 5.13-5.04 (m, 1H), 4.55-4.42 (m, 2H), 4.30-4.20 (m, 2H), 2.48-2.40 (m, 2H), 2.29-2.14 (m, 4H), 1.89-1.74 (m, 2H), 1.60 (br s, 3H), 1.57-1.43 (m, 5H), 1.29-1.14 (m, 24H), 0.89-0.81 (m, 3H), 0.09 (s, 9H).

Example 47 (S)-2-{6,6-Dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl isobutanoate (Compound No. V-1454)

To a solution of 247 mg (0.456 mmol) of (S)-ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 38 in 3 ml of dehydrated dichloromethane, 0.15 ml (1.1 mmol) of triethylamine and 0.060 ml (0.57 mmol) of isobutyryl chloride were added in this order at room temperature in a nitrogen atmosphere and then stirred at the same temperature as above for 100 minutes. Subsequently, 1.0 ml (7.2 mmol) of triethylamine and 1.0 ml (25 mmol) of methanol were added to the reaction solution and then stirred at room temperature for 4.5 hours.

After the completion of the reaction, water was added to the reaction solution, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: dichloromethane:methanol=100:0 to 99:1 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with ethyl acetate/n-hexane, and the obtained solid was collected by filtration, washed by sousing with n-hexane, and then dried under reduced pressure to obtain 202 mg of the title compound (yield: 82%) as a white solid.

Mass spectrum (CI, m/z): 540 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.61 (br s, total 1H), 9.53 (s, 1H), 7.47-7.38 (m, 2H), 7.38-7.29 (m, 2H), 7.29-7.20 (m, 1H), 6.71-6.34 (m, 1H), 5.20-5.03 (m, 1H), 4.57-4.38 (m, 2H), 4.33-4.15 (m, 2H), 2.48-2.42 (m, 3H), 2.27-2.13 (m, 2H), 1.92-1.73 (m, 2H), 1.65-1.47 (m, 6H), 1.08-0.99 (m, 6H), 0.14-0.05 (m, 9H).

Example 48 (S)-2-{6,6-Dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl pivalate (Compound No. V-1462)

To a solution of 210 mg (0.387 mmol) of (S)-ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 38 and 0.11 ml (0.79 mmol) of triethylamine in 3 ml of dehydrated dichloromethane, 0.12 ml (0.59 mmol) of pivalic anhydride and 10.5 mg (0.086 mmol) of 4-dimethylaminopyridine were added in an argon atmosphere and stirred at room temperature for 4.5 hours. Subsequently, 0.5 ml of triethylamine and 1 ml of methanol were added to the reaction solution and reacted at room temperature for 14 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure. Diisopropyl ether was added to the obtained concentration residue, and after ultrasonication, insoluble matter was collected by filtration and dried under reduced pressure to obtain 144 mg of the title compound (yield: 67%) as a white solid.

Mass spectrum (CI, m/z): 554 [M+1]⁺

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.66 (br s, total 1H), 9.55 (s, 1H), 7.45-7.38 (m, 2H), 7.37-7.31 (m, 2H), 7.28-7.22 (m, 1H), 6.68-6.40 (m, 1H), 5.20-5.09 (m, 1H), 4.48 (br s, 2H), 4.29-4.19 (m, 2H), 2.49-2.41 (m, 2H), 2.26-2.14 (m, 2H), 1.90-1.74 (m, 2H), 1.59 (s, 3H), 1.55 (s, 3H), 1.08 (s, 9H), 0.09 (s, 9H).

Example 49 (S)-2-{6,6-Dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl 3-methylbutanoate (Compound No. V-1466)

To a solution of 201 mg (0.371 mmol) of a mixture of (S)-ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate synthesized in the similar manner as in Reference Example 38 and (S)-ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate and 0.10 ml (0.74 mmol) of triethylamine in 3 ml of dichloromethane, 0.11 ml (0.56 mmol) of isovaleric anhydride and 10.6 mg (0.087 mmol) of 4-dimethylaminopyridine were added at room temperature in an argon atmosphere and then reacted at the same temperature as above for 3 hours. Subsequently, 1.0 ml of methanol and 0.5 ml of triethylamine were added and reacted at room temperature for 15.5 hours, then the reaction solution was concentrated under reduced pressure, and 1.0 ml of methanol and 0.5 ml of triethylamine were added again to the obtained concentration residue and reacted at 40° C. for 6 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and 8 ml of ethyl acetate, 0.4 ml of water, and 8 ml of a saturated aqueous solution of sodium chloride were added to the obtained concentration residue, and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with 10 ml of dichloromethane twice, and all of the obtained organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. Diethyl ether was added to the obtained concentration residue, ultrasonicated, and then concentrated under reduced pressure. Water was added to the obtained concentration residue, ultrasonicated, and left standing overnight, and then, insoluble matter was filtered and dried under reduced pressure to obtain 97 mg of the title compound (yield: 47%) as a white solid.

Mass spectrum (CI, m/z): 554 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.50-11.49 (m, 1H), 9.55 (s, 1H), 7.44-7.38 (m, 2H), 7.37-7.30 (m, 2H), 7.29-7.22 (m, 1H), 6.84-6.25 (m, 1H), 5.13-5.06 (m, 1H), 4.55-4.41 (m, 2H), 4.31-4.21 (m, 2H), 2.49-2.42 (m, 2H), 2.26-2.11 (m, 4H), 2.01-1.87 (m, 1H), 1.87-1.74 (m, 2H), 1.59 (s, 3H), 1.53 (s, 3H), 0.87-0.82 (m, 6H), 0.09 (s, 9H).

Example 50 (S)-2-{6,6-Dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl benzoate (Compound No. V-1482)

To a solution of 132 mg (0.244 mmol) of (S)-ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 38 and 0.068 ml (0.49 mmol) of triethylamine in 2.5 ml of dehydrated dichloromethane, 0.042 ml (0.36 mmol) of benzoyl chloride was added at room temperature in an argon atmosphere and stirred at the same temperature as above for 1 hour. Subsequently, 0.5 ml of triethylamine and 0.5 ml of methanol were added to the reaction solution and stirred at room temperature for 20 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 94 mg of the title compound (yield: 67%) as a white solid.

Mass spectrum (CI, m/z): 574 [M+1]⁺

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.19 & 11.71 (br s, total 1H), 9.55 (br s, 1H), 7.95-7.91 (m, 2H), 7.66-7.60 (m, 1H), 7.52-7.46 (m, 4H), 7.39-7.33 (m, 2H), 7.30-7.24 (m, 1H), 6.73-6.59 (m, 1H), 5.35-5.26 (m, 1H), 4.57-4.44 (m, 4H), 2.48-2.42 (m, 2H), 2.23-2.15 (m, 2H), 1.87-1.73 (m, 2H), 1.57 (s, 3H), 1.55 (s, 3H), 0.08 (s, 9H).

Example 51 (S)-2-{6,6-Dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl ethyl carbonate (Compound No. V-1486)

To a solution of 265 mg (0.490 mmol) of (S)-ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 38 in 4 ml of dehydrated dichloromethane, 0.14 ml (1.0 mmol) of triethylamine and 0.060 ml (0.63 mmol) of ethyl chloroformate were added in this order at room temperature in a nitrogen atmosphere and then stirred at the same temperature as above for 2 hours. Then, 0.20 ml (1.4 mmol) of triethylamine and 0.10 ml (1.1 mmol) of ethyl chloroformate were added at room temperature and stirred at the same temperature as above for 1.5 hours. 0.20 ml (1.4 mmol) of triethylamine and 0.10 ml (1.1 mmol) of ethyl chloroformate were further added again at room temperature and stirred at the same temperature as above for 1 hour. Subsequently, 1.0 ml (7.2 mmol) of triethylamine and 1.0 ml (25 mmol) of methanol were added to the reaction solution and then stirred at room temperature for 4 hours.

After the completion of the reaction, water was added to the reaction solution, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: dichloromethane:methanol=100:0 to 98:2 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected to preparative HPLC (column: X-Bridge (trade name) ODS, elution solvent: acetonitrile:1 mM aqueous dipotassium hydrogen phosphate solution=45:55 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, and acetonitrile was distilled off. The deposited solid was collected by filtration, washed by sousing with pure water, and then dried under reduced pressure to obtain 60 mg of the title compound (yield: 23%) as a white solid.

Mass spectrum (ESI, m/z): 542 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.65 (br s, total 1H), 9.62-9.49 (m, 1H), 7.44-7.31 (m, 4H), 7.28-7.21 (m, 1H), 6.68-6.45 (m, 1H), 5.21-4.99 (m, 1H), 4.59-4.40 (m, 2H), 4.38-4.22 (m, 2H), 4.10 (q, J=7.0 Hz, 2H), 2.56-2.42 (m, 2H), 2.27-2.14 (m, 2H), 1.93-1.73 (m, 2H), 1.69-1.45 (m, 6H), 1.18 (t, J=7.0 Hz, 3H), 0.17-0.04 (m, 9H).

Example 52 Sodium (S)-4-(2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethoxy)-4-oxobutanoate (sodium salt of Compound No. V-1490)

To a solution of 201 mg (0.456 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 7.0 ml of 1,4-dioxane, 628 mg of (S)-2-amino-2-phenylethyl benzyl succinate trifluoroacetate (containing impurities) synthesized in the similar manner as in Reference Example 40 and 1.0 ml (5.7 mmol) of DIPEA were added, applied to a microwave reaction apparatus, and reacted at 100° C. for 1 hour. Subsequently, 1 ml of methanol and 1 ml of triethylamine were added, applied to a microwave reaction apparatus, and reacted at 80° C. for 3 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, ethyl acetate was added to the obtained concentration residue, washed with a 10% aqueous potassium dihydrogen phosphate solution, water, a saturated aqueous solution of sodium bicarbonate, and a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous magnesium sulfate, and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=100:0 to 70:30 (V/V)), and a fraction containing (S)-benzyl (2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethyl)succinate was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 171 mg of the obtained concentration residue in 20 ml of ethanol, 25.4 mg of palladium/carbon (ASCA2 (trade name), manufactured by N.E. Chemcat Corp., containing 52% water) was added in a nitrogen atmosphere and then, after replacement with a hydrogen atmosphere under reduced pressure, stirred at room temperature for 2 hours.

After the completion of the reaction, replacement with an argon atmosphere was performed, and the reaction solution was filtered through celite. 0.26 ml (0.26 mmol) of a 1 N aqueous sodium hydroxide solution was added to the filtrate and concentrated under reduced pressure. Diethyl ether was added to the obtained residue and then ultrasonicated, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 147 mg of the title compound (yield: 54% [2 steps]) as a white solid.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 13.32 (br s, 1H), 10.75 (br s, 1H), 7.44-7.38 (m, 2H), 7.36-7.29 (m, 2H), 7.28-7.19 (m, 1H), 6.47 (d, J=7.3 Hz, 1H), 5.11-5.02 (m, 1H), 4.57-4.41 (m, 2H), 4.28 (dd, J=5.6, 10.8 Hz, 1H), 4.17 (dd, J=8.0, 10.8 Hz, 1H), 2.49-2.42 (m, 2H), 2.35 (t, J=7.2 Hz, 2H), 2.25-2.16 (m, 2H), 2.11 (t, J=7.2 Hz, 2H), 1.87-1.71 (m, 2H), 1.58 (s, 3H), 1.51 (s, 3H), 0.08 (s, 9H).

Example 53 (S)-(2-{6,6-Dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylethoxy)methyl pivalate (Compound No. VI-474)

To a solution of 272 mg (1.08 mmol) of (S)-(2-amino-2-phenylethoxy)methyl pivalate synthesized in the similar manner as in Reference Example 42 in 2 ml of dehydrated THF, 0.15 ml (0.86 mmol) of DIPEA and 162 mg (0.368 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 were added in this order at room temperature in a nitrogen atmosphere and then stirred for 130 minutes while heated to reflux. Subsequently, 1.0 ml of triethylamine and 0.8 ml of methanol were added to the reaction solution and then stirred for 70 minutes while heated to reflux.

After the completion of the reaction, water was added to the reaction solution, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DNH silica gel, elution solvent: dichloromethane:methanol=100:0 to 98:2 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with ethyl acetate/n-hexane, and the deposited solid was collected by filtration, washed by sousing with n-hexane, and then dried under reduced pressure to obtain 176 mg of the title compound (yield: 82%) as a white solid.

Mass spectrum (CI, m/z): 584 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.64 (br s, total 1H), 9.59-9.49 (m, 1H), 7.41-7.35 (m, 2H), 7.35-7.27 (m, 2H), 7.25-7.19 (m, 1H), 6.42 & 6.28 (d, J=8.0 Hz, total 1H), 5.29 (d, J=6.2 Hz, 1H), 5.22 (d, J=6.2 Hz, 1H), 5.02-4.94 (m, 1H), 4.57-4.37 (m, 2H), 3.91-3.83 (m, 1H), 3.79 (dd, J=6.0, 10.0 Hz, 1H), 2.49-2.40 (m, 2H), 2.28-2.13 (m, 2H), 1.92-1.73 (m, 2H), 1.67-1.45 (m, 6H), 1.13 (s, 9H), 0.14-0.06 (m, 9H).

Example 54 (S)-2-Acetoxy-1-phenylethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate (Compound No. V-1250)

To a solution of 412 mg of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate (containing impurities) synthesized in the similar manner as in Reference Example 3 by using 506 mg (1.06 mmol) of 5-tert-butyl 2-ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]pyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate synthesized in the similar manner as in Reference Example 84 in 4 ml of dehydrated THF, 0.70 ml (4.0 mmol) of DIPEA and 1.30 g (3.84 mmol) of (S)-2-({[(2,5-dioxopyrrolidin-1-yl)oxy]carbonyl}oxy)-2-phenylethyl acetate synthesized in the similar manner as in Reference Example 43 were added in this order at room temperature in a nitrogen atmosphere and then stirred for 1.5 hours while heated to reflux. Subsequently, 2.0 ml (14 mmol) of triethylamine and 1.5 ml (37 mmol) of methanol were added to the reaction solution and then stirred for 3.5 hours while heated to reflux.

After the completion of the reaction, water was added to the reaction solution, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=80:20 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 225 mg of a concentration residue.

Approximately 50 mg of the obtained concentration residue was subjected to preparative HPLC (column: X-Bridge (trade name) ODS, elution solvent: acetonitrile:1 mM aqueous dipotassium hydrogen phosphate solution=50:50 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, and acetonitrile was distilled off. The concentration residue was subjected to extraction with ethyl acetate twice, and all of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with ethyl acetate/diisopropyl ether/n-hexane, and the deposited solid was collected by filtration, washed by sousing with n-hexane, and then dried under reduced pressure to obtain 11.6 mg of the title compound (yield: 2% [2 steps]) as a white solid.

Mass spectrum (CI, m/z): 513 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.35-12.21 & 11.97-11.83 (m, total 1H), 9.87-9.45 (m, 1H), 7.47-7.24 (m, 5H), 5.99-5.85 (m, 1H), 4.65-4.17 (m, 4H), 2.48-2.36 (m, 2H), 2.28-2.10 (m, 2H), 2.05-1.95 (m, 3H), 1.92-1.72 (m, 2H), 1.71-1.43 (m, 6H), 0.16-0.02 (m, 9H).

Example 55 (S)-Benzyl 2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylacetate (Compound No. IV-411)

To a solution of 195 mg (0.442 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 7 ml of 1,4-dioxane, 565 mg of (S)-benzyl 2-amino-2-phenylacetate trifluoroacetate (containing impurities) synthesized in the similar manner as in Reference Example 45 and 0.50 ml (2.9 mmol) of DIPEA were added at room temperature in an argon atmosphere, then applied to a microwave reaction apparatus, and stirred at 100° C. for 1 hour. After the reaction, the reaction solution was concentrated under reduced pressure, and 4 ml of methanol and 1 ml of triethylamine were added to the obtained concentration residue, applied to a microwave reaction apparatus, and reacted at 80° C. for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, ethyl acetate was added to the obtained concentration residue, the organic layer after washing with a 10% aqueous potassium dihydrogen phosphate solution, a saturated aqueous solution of sodium bicarbonate, and a saturated aqueous solution of sodium chloride in this order was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=100:0 to 55:45 (V/V)), and a fraction composed mainly of the title compound and a fraction composed mainly of a by-product [(S)-methyl 2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylacetate] were each concentrated under reduced pressure. The concentration residue of the fraction composed mainly of the title compound was subjected again to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=100:0 to 55:45 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 99 mg of the title compound (yield: 39%) as a white foam.

Mass spectrum (DUIS, m/z): 574 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.70 (br s, total 1H), 9.63-9.44 (m, 1H), 7.51-7.41 (m, 2H), 7.38-7.23 (m, 8H), 6.81-6.47 (m, 1H), 5.42 (d, J=7.2 Hz, 1H), 5.17 (d, J=12.7 Hz, 1H), 5.11 (d, J=12.7 Hz, 1H), 4.61-4.39 (m, 2H), 2.49-2.38 (m, 2H), 2.25-2.12 (m, 2H), 1.91-1.72 (m, 2H), 1.68-1.52 (m, 6H), 0.07 (s, 9H).

Example 56 (S)-Methyl 2-{6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazole-5-carboxamido}-2-phenylacetate (Compound No. IV-419)

The concentration residue of the fraction composed mainly of the title compound collected at the time of the first purification of silica gel column chromatography in the operational steps of Example 55 was subjected again to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=100:0 to 55:45 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 29 mg of the title compound (yield: 13%) as a white foam.

Mass spectrum (DUIS, m/z): 498 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.71 (br s, total 1H), 9.63-9.46 (m, 1H), 7.48-7.41 (m, 2H), 7.40-7.28 (m, 3H), 6.73-6.56 (m, 1H), 5.36 (d, J=7.2 Hz, 1H), 4.61-4.38 (m, 2H), 3.62 (s, 3H), 2.49-2.38 (m, 2H), 2.27-2.10 (m, 2H), 1.92-1.71 (m, 2H), 1.67-1.51 (m, 6H), 0.08 (s, 9H).

Example 57 N-(2,2-Difluoro-3-hydroxy-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-362)

To a solution of 249 mg (1.33 mmol) of 3-amino-2,2-difluoro-3-phenylpropan-1-ol synthesized in the similar manner as in Reference Example 48 in 2 ml of dehydrated 1,4-dioxane, 0.30 ml (1.7 mmol) of DIPEA and 178 mg (0.403 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 were added in this order at room temperature in a nitrogen atmosphere and then stirred at 80° C. for 7 hours. Subsequently, 0.10 ml (1.7 mmol) of 2-aminoethanol was added to the reaction solution allowed to cool to room temperature, and then stirred at room temperature for 1.5 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred, followed by extraction with dichloromethane three times. All of the organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 155 mg of the title compound (yield: 74%) as a white solid.

Mass spectrum (CI, m/z): 520 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.43-11.84 (m, 1H), 10.02-9.36 (m, 1H), 7.56-7.50 (m, 2H), 7.40-7.27 (m, 3H), 6.61 (br s, 1H), 5.71 (br s, 1H), 5.49-5.34 (m, 1H), 4.70-4.56 (m, 1H), 4.47 (br d, J=12.0 Hz, 1H), 3.73-3.45 (m, 2H), 2.57-2.42 (m, 2H), 2.26-2.15 (m, 2H), 1.90-1.74 (m, 2H), 1.61 (s, 3H), 1.51 (s, 3H), 0.09 (s, 9H).

Example 58 N-(2-Isopropoxy-1-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-146)

To a solution of 0.102 g (0.231 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 and 0.127 g (0.709 mmol) of 2-isopropoxy-1-phenylethanamine synthesized in the similar manner as in Reference Example 50 in 2.5 ml of dehydrated 1,4-dioxane, 0.200 ml (1.15 mmol) of DIPEA was added at room temperature in a nitrogen atmosphere and then heated and stirred at 100° C. for 1 hour. After standing to cool, 0.50 ml (12 mmol) of methanol and 0.070 ml (1.2 mmol) of 2-aminoethanol were added to the reaction solution and stirred at room temperature for 1 hour.

After the completion of the reaction, ethyl acetate was added to the residue obtained by concentration under reduced pressure, the organic layer after washing with a 10% aqueous potassium dihydrogen phosphate solution, a saturated aqueous solution of sodium bicarbonate, and a saturated aqueous solution of sodium chloride in this order was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=100:0 to 50:50 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, the residue was dissolved in a small amount of dichloromethane, and after addition of n-hexane and ultrasonication, the deposited solid was collected by filtration and dried under reduced pressure to obtain 0.106 g of the title compound (yield: 90%) as a white solid.

Mass spectrum (CI, m/z): 512 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.76 (br s, total 1H), 9.68-9.50 (m, 1H), 7.42-7.16 (m, 5H), 6.31-6.08 (m, 1H), 4.94-4.84 (m, 1H), 4.56-4.37 (m, 2H), 3.67-3.51 (m, 3H), 2.51-2.40 (m, 2H), 2.27-2.13 (m, 2H), 1.92-1.71 (m, 2H), 1.65-1.48 (m, 6H), 1.08-1.03 (m, 6H), 0.09 (s, 9H).

Example 59 6,6-Dimethyl-N-(2-phenoxy-1-phenylethyl)-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-162)

To a solution of 0.101 g (0.230 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 and 0.145 g (0.681 mmol) of 2-phenoxy-1-phenylethanamine synthesized in the similar manner as in Reference Example 52 in 2.5 ml of dehydrated 1,4-dioxane, 0.200 ml (1.15 mmol) of DIPEA was added at room temperature in a nitrogen atmosphere and then stirred at 100° C. for 1 hour. After standing to cool, 0.50 ml (12 mmol) of methanol and 0.070 ml (1.2 mmol) of 2-aminoethanol were added and stirred at room temperature for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, ethyl acetate was added, the organic layer after washing with a 10% aqueous potassium dihydrogen phosphate solution, a saturated aqueous solution of sodium bicarbonate, and a saturated aqueous solution of sodium chloride in this order was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=100:0 to 67:33 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, the residue was dissolved in a small amount of dichloromethane, and after addition of n-hexane and ultrasonication, the deposited solid was collected by filtration and dried under reduced pressure to obtain 0.112 g of the title compound (yield: 89%) as a white solid.

Mass spectrum (CI, m/z): 546 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.70 (br s, total 1H), 9.57 (br s, 1H), 7.51-7.18 (m, 7H), 7.03-6.86 (m, 3H), 6.68-6.40 (m, 1H), 5.23-5.11 (m, 1H), 4.57-4.38 (m, 2H), 4.34-4.22 (m, 1H), 4.16 (dd, J=5.9, 9.8 Hz, 1H), 2.57-2.39 (m, 2H), 2.25-2.11 (m, 2H), 1.90-1.71 (m, 2H), 1.62 (br s, 3H), 1.54 (br s, 3H), 0.08 (s, 9H).

Example 60 (S)—N-[1-(2-Chlorophenyl)-2-hydroxyethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-959)

To a solution of 0.105 g (0.238 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 and 0.124 g (0.723 mmol) of (S)-2-amino-2-(2-chlorophenyl)ethanol [purchased from Amatek Chemical Co., Ltd.] in 2.5 ml of dehydrated 1,4-dioxane, 0.200 ml (1.15 mmol) of DIPEA was added at room temperature in a nitrogen atmosphere and then stirred at 100° C. for 1 hour. After standing to cool, 0.50 ml (12 mmol) of methanol and 0.070 ml (1.2 mmol) of 2-aminoethanol were added and stirred at room temperature for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, ethyl acetate was added to the residue, the organic layer after washing with a 10% aqueous potassium dihydrogen phosphate solution, a saturated aqueous solution of sodium bicarbonate, and a saturated aqueous solution of sodium chloride in this order was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=84:16 to 33:67 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, the residue was dissolved in a small amount of dichloromethane, and after addition of n-hexane and ultrasonication, the deposited solid was collected by filtration and dried under reduced pressure to obtain 0.0958 g of the title compound (yield: 80%) as a white solid.

Mass spectrum (DUIS, m/z): 504 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.75 (br s, total 1H), 9.71-9.52 (m, 1H), 7.51 (dd, J=1.6, 7.7 Hz, 1H), 7.38 (dd, J=1.2, 7.8 Hz, 1H), 7.33-7.20 (m, 2H), 6.36-6.14 (m, 1H), 5.21-5.12 (m, 1H), 5.04 (t, J=6.0 Hz, 1H), 4.66-4.45 (m, 2H), 3.64-3.48 (m, 2H), 2.57-2.41 (m, 2H), 2.28-2.13 (m, 2H), 1.91-1.72 (m, 2H), 1.66-1.42 (m, 6H), 0.10 (s, 9H).

Example 61 (S)—N-[2-Hydroxy-1-(o-tolyl)ethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-1067)

To a solution of 0.104 g (0.235 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 and 0.131 g (0.696 mmol) of (S)-2-amino-2-(o-tolyl)ethanol hydrochloride [purchased from Acesys Pharmatech Ltd.] in 2.5 ml of dehydrated 1,4-dioxane, 0.400 ml (2.30 mmol) of DIPEA was added at room temperature in a nitrogen atmosphere and then heated and stirred at 100° C. for 1 hour. After standing to cool, 0.50 ml (12 mmol) of methanol and 0.070 ml (1.2 mmol) of 2-aminoethanol were added and stirred at room temperature for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, ethyl acetate was added, the organic layer after washing with a 10% aqueous potassium dihydrogen phosphate solution, a saturated aqueous solution of sodium bicarbonate, and a saturated aqueous solution of sodium chloride in this order was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=84:16 to 33:67 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, the residue was dissolved in a small amount of dichloromethane, and after addition of n-hexane and ultrasonication, the deposited solid was collected by filtration and dried under reduced pressure to obtain 0.0738 g of the title compound (yield: 65%) as a white solid.

Mass spectrum (CI, m/z): 484 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.66 (br s, total 1H), 9.63-9.50 (m, 1H), 7.40 (d, J=7.4 Hz, 1H), 7.18-7.03 (m, 3H), 6.28-6.05 (m, 1H), 5.04-4.95 (m, 1H), 4.89 (t, J=6.0 Hz, 1H), 4.58-4.41 (m, 2H), 3.61-3.43 (m, 2H), 2.56-2.41 (m, 2H), 2.36 (s, 3H), 2.27-2.11 (m, 2H), 1.93-1.70 (m, 2H), 1.69-1.41 (m, 6H), 0.10 (s, 9H).

Example 62 (S)—N-(1-Hydroxy-3-phenylpropan-2-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-862)

To a solution of 101 mg (0.229 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 3 ml of 1,4-dioxane, 0.115 ml (0.673 mmol) of DIPEA and 102 mg (0.675 mmol) of (S)-2-amino-3-phenylpropan-1-ol were added in this order in an argon atmosphere and then stirred at 100° C. for 1 hour. Subsequently, the reaction solution was concentrated under reduced pressure, and 2 ml of methanol and 0.5 ml of triethylamine were added in this order at room temperature and stirred at 80° C. for 1 hour in a microwave reaction apparatus.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, the concentration residue was dissolved in 5 ml of ethyl acetate and washed with a 5% aqueous potassium dihydrogen phosphate solution twice, and then, the organic layer was washed with 5 ml of a saturated aqueous solution of sodium bicarbonate. The organic layer was dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: ethyl acetate:methanol=100:0 to 86:14 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and subsequently dried under reduced pressure at 50° C. to obtain 88.5 mg of the title compound (yield: 80%) as a white solid.

Mass spectrum (CI, m/z): 484 [M+1]+.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.19 & 11.71 (br s, total 1H), 9.54 (br s, 1H), 7.28-7.18 (m, 4H), 7.18-7.12 (m, 1H), 5.72-5.45 (m, 1H), 4.77 (t, J=5.5 Hz, 1H), 4.46-4.17 (m, 2H), 3.90-3.77 (m, 1H), 3.44-3.28 (m, 2H), 2.87-2.70 (m, 2H), 2.54-2.40 (m, 2H), 2.25-2.13 (m, 2H), 1.92-1.70 (m, 2H), 1.58 (br s, 3H), 1.50 (br s, 3H), 0.09 (s, 9H).

Example 63 N-(2-Hydroxy-3-methylbutyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-446)

To a solution of 103 mg (0.234 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 3 ml of 1,4-dioxane, 69.8 mg (0.677 mmol) of 1-amino-3-methylbutan-2-ol [purchased from Life Chemicals Inc.] and 0.115 ml (0.673 mmol) of DIPEA were added in this order at room temperature in an argon atmosphere and then stirred at 100° C. for 2.5 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, the concentration residue was dissolved in 5 ml of ethyl acetate and washed with a 5% aqueous potassium dihydrogen phosphate solution twice, and then, the organic layer was washed with 5 ml of a saturated aqueous solution of sodium bicarbonate. The organic layer was dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: ethyl acetate:methanol=100:0 to 86:14 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in dichloromethane, n-hexane was added, and then, the deposited solid was collected by filtration and dried under reduced pressure to obtain 71.9 mg of the title compound (yield: 71%) as a white solid.

Mass spectrum (CI, m/z): 436 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.72 (br s, total 1H), 9.56 (br s, 1H), 6.03-5.75 (m, 1H), 4.79 (d, J=4.5 Hz, 1H), 4.48-4.27 (m, 2H), 3.29-3.17 (m, 2H), 2.96-2.85 (m, 1H), 2.56-2.39 (m, 2H), 2.25-2.12 (m, 2H), 1.91-1.72 (m, 2H), 1.68-1.50 (m, 7H), 0.86 (d, J=6.8 Hz, 6H), 0.08 (s, 9H).

Example 64 (R)—N-(1-Hydroxy-3-phenylpropan-2-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-861)

To a solution of 0.102 g (0.232 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 and 0.110 g (0.729 mmol) of (R)-2-amino-3-phenylpropan-1-ol in 2.5 ml of dehydrated 1,4-dioxane, 0.20 ml (1.1 mmol) of DIPEA was added at room temperature in an argon atmosphere and then heated and stirred at 100° C. for 1.5 hours. After standing to cool, the resultant was concentrated under reduced pressure, and 4 ml of methanol and 1 ml of triethylamine were added to the residue, applied to a microwave reaction apparatus, and reacted at 80° C. for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, ethyl acetate was added, the organic layer after washing with a 10% aqueous potassium dihydrogen phosphate solution, a saturated aqueous solution of sodium bicarbonate, and a saturated aqueous solution of sodium chloride in this order was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: ethyl acetate:methanol=100:0 to 90:10 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, small amounts of dichloromethane and n-hexane were added to the residue, and after ultrasonication, the deposited solid was collected by filtration and dried under reduced pressure to obtain 0.0454 g of the title compound (yield: 40%) as a white solid.

Mass spectrum (CI, m/z): 484 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.19 & 11.65 (br s, total 1H), 9.54 (s, 1H), 7.28-7.18 (m, 4H), 7.18-7.12 (m, 1H), 5.70-5.47 (m, 1H), 4.77 (t, J=5.5 Hz, 1H), 4.45-4.19 (m, 2H), 3.90-3.77 (m, 1H), 3.46-3.29 (m, 2H), 2.87-2.70 (m, 2H), 2.56-2.38 (m, 2H), 2.26-2.11 (m, 2H), 1.92-1.71 (m, 2H), 1.65-1.40 (m, 6H), 0.09 (s, 9H).

Example 65 (R)—N-(2-Hydroxy-2-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-786)

To a solution of 101 mg (0.229 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 2 ml of dehydrated THF, 0.20 ml (1.1 mmol) of DIPEA and 151 mg (1.10 mmol) of (R)-2-amino-1-phenylethanol were added in this order at room temperature in a nitrogen atmosphere and then stirred for 3 hours then with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred, followed by extraction with dichloromethane three times. All of the organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=70:30 to 20:80 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected to preparative HPLC (column: X-Bridge (trade name) ODS, elution solvent: acetonitrile:1 mM aqueous dipotassium hydrogen phosphate solution=40:60 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, and acetonitrile was distilled off. The solid deposited in the course of concentration was collected by filtration, washed with pure water, and then dried under reduced pressure to obtain 55 mg of the title compound (yield: 51%) as a white solid.

Mass spectrum (EI, m/z): 469 [M]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.67 (br s, total 1H), 9.56 (s, 1H), 7.36-7.28 (m, 4H), 7.27-7.19 (m, 1H), 6.19-5.94 (m, 1H), 5.59 (d, J=4.0 Hz, 1H), 4.66 (td, J=4.0, 8.0 Hz, 1H), 4.48-4.24 (m, 2H), 3.44-3.22 (m, 1H), 3.09 (ddd, J=4.8, 8.0, 13.2 Hz, 1H), 2.56-2.38 (m, 2H), 2.26-2.12 (m, 2H), 1.90-1.72 (m, 2H), 1.60 (br s, 6H), 0.08 (s, 9H).

Example 66 (S)—N-(2-Hydroxy-2-phenylethyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-787)

To a solution of 102 mg (0.231 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 2 ml of dehydrated THF, 0.20 ml (1.1 mmol) of DIPEA and 129 mg (0.943 mmol) of (S)-2-amino-1-phenylethanol were added in this order at room temperature in a nitrogen atmosphere and then stirred for 4 hours with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred, followed by extraction with dichloromethane three times. All of the organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: dichloromethane:methanol=100:0 to 98:2 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected to preparative HPLC (column: X-Bridge (trade name) ODS, elution solvent: acetonitrile:1 mM aqueous dipotassium hydrogen phosphate solution=45:55 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, and acetonitrile was distilled off. The solid deposited in the course of concentration was collected by filtration, washed with pure water, and then dried under reduced pressure. Ethyl acetate was added to the obtained solid, then insoluble matter was removed by filtration, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 52 mg of the title compound (yield: 48%) as a white solid.

Mass spectrum (EI, m/z): 469 [M]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.70 (br s, total 1H), 9.63-9.53 (m, 1H), 7.36-7.28 (m, 4H), 7.27-7.19 (m, 1H), 6.19-5.94 (m, 1H), 5.59 (d, J=4.0 Hz, 1H), 4.66 (td, J=4.0, 8.0 Hz, 1H), 4.48-4.24 (m, 2H), 3.44-3.22 (m, 1H), 3.15-3.04 (m, 1H), 2.56-2.38 (m, 2H), 2.26-2.12 (m, 2H), 1.90-1.72 (m, 2H), 1.60 (br s, 6H), 0.08 (s, 9H).

Example 67 2-Hydroxy-2-phenylethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate (Compound No. IV-670)

To a solution of 0.125 g of 2-[(2-methoxypropan-2-yl)oxy]-2-phenylethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate (containing impurities) synthesized in Reference Example 56 in 3 ml of methanol, 0.0077 g (0.031 mmol) of pyridinium p-toluenesulfonate was added at 0° C. in a nitrogen atmosphere and stirred at the same temperature as above for 3.5 hours, and then, 0.020 ml of triethylamine was added and concentrated under reduced pressure.

The residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=77:23 to 26:74 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 0.0837 g of the title compound (yield: 66% [2 steps]) as a white foam.

Mass spectrum (CI, m/z): 471 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.25 & 12.19 & 11.83 (br s, total 1H), 9.73-9.49 (m, 1H), 7.47-7.19 (m, 5H), 5.58 (d, J=4.5 Hz, 1H), 4.89-4.74 (m, 1H), 4.50-4.23 (m, 2H), 4.21-3.91 (m, 2H), 2.57-2.35 (m, 2H), 2.27-2.09 (m, 2H), 1.93-1.68 (m, 2H), 1.66-1.30 (m, 6H), 0.17-0.01 (m, 9H).

Example 68 (R)—N-[6,6-Dimethyl-5-(2-phenoxypropanoyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1258)

To a solution of 58.3 mg (0.351 mmol) of (R)-2-phenoxypropanoic acid in 2 ml of dehydrated DMF, 0.12 ml (0.69 mmol) of DIPEA and 152 mg (0.354 mmol) of (1-cyano-2-ethoxy-2-oxoethylideneaminooxy)dimethylaminomorpholinocarbenium hexafluorophosphate [COMU (trade name)] were added in this order at 0° C. in a nitrogen atmosphere and then stirred for 20 minutes with the temperature unchanged. Subsequently, 104 mg (0.274 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate synthesized in the similar manner as in Reference Example 5 was added at 0° C. and then stirred at room temperature for 15.5 hours. Subsequently, 0.10 ml (1.7 mmol) of 2-aminoethanol was added to the reaction solution at room temperature and then stirred for 2.5 hours with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The operation of adding toluene to the obtained concentration residue, followed by concentration under reduced pressure again was repeated twice, then the resultant was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=75:25 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 75 mg of the title compound (yield: 60%) as a white solid.

Mass spectrum (EI, m/z): 454 [M]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.53-11.80 (m, 1H), 9.69 (br s, 1H), 7.30-7.21 (m, 2H), 6.94-6.87 (m, 1H), 6.85-6.78 (m, 2H), 4.90 (q, J=6.5 Hz, 1H), 4.87-4.78 (m, 1H), 4.67-4.57 (m, 1H), 2.56-2.38 (m, 2H), 2.25-2.12 (m, 2H), 1.87-1.74 (m, 2H), 1.67-1.58 (m, 6H), 1.46 (d, J=6.5 Hz, 3H), 0.06 (s, 9H).

Example 69 (S)—N-[6,6-Dimethyl-5-(2-phenoxypropanoyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1259)

To a solution of 58.6 mg (0.353 mmol) of (S)-2-phenoxypropanoic acid in 2 ml of dehydrated DMF, 0.12 ml (0.69 mmol) of DIPEA and 153 mg (0.356 mmol) of (1-cyano-2-ethoxy-2-oxoethylideneaminooxy)dimethylaminomorpholinocarbenium hexafluorophosphate [COMU (trade name)] were added in this order at 0° C. in a nitrogen atmosphere and then stirred for 20 minutes with the temperature unchanged. Subsequently, 104 mg (0.275 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate synthesized in the similar manner as in Reference Example 5 was added at 0° C. and then stirred at room temperature for 3 hours. Subsequently, 0.10 ml (1.7 mmol) of 2-aminoethanol was added to the reaction solution at room temperature and then stirred for 2 hours with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The operation of adding toluene to the obtained concentration residue, followed by concentration under reduced pressure again was repeated twice, then the resultant was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=75:25 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 75 mg of the title compound (yield: 60%) as a white solid.

Mass spectrum (EI, m/z): 454 [M]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.32 & 11.92 (br s, total 1H), 9.81-9.55 (m, 1H), 7.30-7.21 (m, 2H), 6.94-6.87 (m, 1H), 6.85-6.78 (m, 2H), 4.96-4.74 (m, 2H), 4.71-4.54 (m, 1H), 2.56-2.38 (m, 2H), 2.26-2.10 (m, 2H), 1.91-1.72 (m, 2H), 1.69-1.54 (m, 6H), 1.46 (d, J=6.5 Hz, 3H), 0.06 (br s, 9H).

Example 70 N-[6,6-Dimethyl-5-(2-phenoxyacetyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1238)

To a solution of 0.143 g (0.279 mmol) of ethyl 6,6-dimethyl-5-(2-phenoxyacetyl)-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 57 in 3 ml of methanol, 0.150 ml (1.38 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature in a nitrogen atmosphere and then stirred at room temperature for 30 minutes.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, ethyl acetate was added to the residue, the organic layer after washing with a 10% aqueous potassium dihydrogen phosphate solution, a saturated aqueous solution of sodium bicarbonate, and a saturated aqueous solution of sodium chloride in this order was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=100:0 to 62:38 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, the residue was dissolved in a small amount of dichloromethane, and after addition of n-hexane and ultrasonication, the deposited solid was collected by filtration and dried under reduced pressure to obtain 0.0876 g of the title compound (yield: 71%) as a white solid.

Mass spectrum (CI, m/z): 441 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.29 & 11.89 (br s, total 1H), 9.84-9.56 (m, 1H), 7.30-7.24 (m, 2H), 6.95-6.89 (m, 3H), 4.78 (s, 2H), 4.73-4.56 (m, 2H), 2.56-2.35 (m, 2H), 2.27-2.08 (m, 2H), 1.93-1.54 (m, 8H), 0.08 (s, 9H).

Example 71 (R)—N-[6,6-Dimethyl-5-(2-phenoxypropanoyl)-1,4,5,6-tetrahydropyrrol o[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclopropanecarboxamide (Compound No. III-1140)

To a solution of 143 mg (0.861 mmol) of (R)-2-phenoxypropanoic acid in 3 ml of dehydrated dichloromethane, 0.12 ml (1.4 mmol) of oxalyl chloride and 0.0050 ml (0.065 mmol) of dehydrated DMF were added in this order at 0° C. in a nitrogen atmosphere and then stirred for 2 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 154 mg (0.424 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 46 and 0.38 ml (2.2 mmol) of DIPEA in 2 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added at 0° C. in a nitrogen atmosphere and then stirred for 1.5 hours with the temperature unchanged. Subsequently, 0.24 ml (2.2 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at 0° C. and then stirred at room temperature for 2 hours.

After the completion of the reaction, the reaction solution diluted with dichloromethane was washed with a 5% aqueous potassium bisulfate solution and then separated into an aqueous layer and an organic layer. The aqueous layer was subjected to extraction with dichloromethane twice, and then, all of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=80:20 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 155 mg of the title compound (yield: 83%) as a white solid.

Mass spectrum (CI, m/z): 441 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.33 & 12.02 (br s, total 1H), 10.03-9.76 (m, 1H), 7.30-7.22 (m, 2H), 6.94-6.87 (m, 1H), 6.85-6.78 (m, 2H), 4.95-4.70 (m, 2H), 4.67-4.51 (m, 1H), 1.70-1.52 (m, 6H), 1.45 (d, J=6.4 Hz, 3H), 0.98 (br s, 2H), 0.80-0.59 (m, 2H), 0.01 (br s, 9H).

Example 72 N-{5-[3-(Benzyloxy)-2-phenoxypropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1354)

To a solution of 340 mg of 3-(benzyloxy)-2-phenoxypropanoic acid (containing impurities) synthesized in the similar manner as in Reference Example 60 in 3 ml of dehydrated dichloromethane, 0.005 ml (0.07 mmol) of DMF and 0.140 ml (1.63 mmol) of oxalyl chloride were added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 236 mg (0.625 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.550 ml (3.16 mmol) of DIPEA in 3 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 1 hour. Subsequently, 0.340 ml (3.12 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then reacted with stirring at room temperature for 16 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel column chromatography (DNH silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 90:10), and some fractions containing the compound of interest at high purity were concentrated under reduced pressure. The obtained concentration residue was dissolved by adding methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 11.7 mg of the title compound (yield: 3.3%) as a white solid. Also, the remaining fractions containing the compound of interest obtained by silica gel column chromatography were combined, concentrated under reduced pressure, and dried under reduced pressure to obtain 162 mg of the title compound (yield: 46%) as a white solid.

Mass spectrum (CI, m/z): 561 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.30 & 11.92 (br s, total 1H), 9.82-9.54 (m, 1H), 7.38-7.20 (m, 7H), 6.97-6.88 (m, 1H), 6.88-6.80 (m, 2H), 5.03-4.66 (m, 3H), 4.60 (s, 2H), 3.93-3.81 (m, 2H), 2.57-2.39 (m, 2H), 2.29-2.11 (m, 2H), 1.91-1.71 (m, 2H), 1.70-1.50 (m, 6H), 0.07 (s, 9H).

Example 73 N-[5-(3-Hydroxy-2-phenoxypropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1330)

To a solution of 162 mg (0.289 mmol) of N-{5-[3-(benzyloxy)-2-phenoxypropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide synthesized in the similar manner as in Example 72 in 5 ml of ethanol, 30 mg of 20% palladium hydroxide/carbon (containing 50 wt % water) was added in an argon atmosphere and after replacement with a hydrogen atmosphere under reduced pressure, stirred at room temperature for 5 hours.

After the completion of the reaction, replacement with an argon atmosphere was performed, and the reaction solution was filtered through celite. The solid on the celite was washed with ethanol, and all of the filtrates were concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 61 mg of the title compound (yield: 45%) as a white solid.

Mass spectrum (CI, m/z): 471 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.39-11.82 (m, 1H), 9.70 (br s, 1H), 7.32-7.22 (m, 2H), 6.95-6.88 (m, 1H), 6.85-6.78 (m, 2H), 5.34-5.23 (m, 1H), 4.92-4.82 (m, 1H), 4.81-4.69 (m, 2H), 3.85-3.71 (m, 2H), 2.60-2.39 (m, 2H), 2.26-2.12 (m, 2H), 1.89-1.71 (m, 2H), 1.62 (s, 3H), 1.60 (s, 3H), 0.08 (s, 9H).

Example 74 N-{5-[2-(4-Chlorophenoxy)propanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1270)

To a solution of 150 mg (0.748 mmol) of 2-(4-chlorophenoxy)propanoic acid [purchased from AK Scientific, Inc.] in 3 ml of dehydrated dichloromethane, 0.080 ml (0.93 mmol) of oxalyl chloride and 0.004 ml (0.05 mmol) of DMF were added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 129 mg (0.341 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.300 ml (1.72 mmol) of DIPEA in 3 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 3 hours. Subsequently, 0.200 ml (1.84 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then reacted with stirring at room temperature for 16 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain a solid. The obtained solid was subjected again to silica gel column chromatography (DNH silica gel, elution solvent: n-hexane:ethyl acetate=50:50 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 39 mg of the title compound (yield: 23%) as a white solid.

Mass spectrum (CI, m/z): 489 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.32 & 11.89 (br s, total 1H), 9.79-9.53 (m, 1H), 7.34-7.24 (m, 2H), 6.90-6.77 (m, 2H), 4.93 (q, J=6.4 Hz, 1H), 4.90-4.72 (m, 1H), 4.70-4.50 (m, 1H), 2.60-2.36 (m, 2H), 2.28-2.10 (m, 2H), 1.93-1.70 (m, 2H), 1.70-1.53 (m, 6H), 1.46 (d, J=6.4 Hz, 3H), 0.06 (s, 9H).

Example 75 N-{5-[2-(2-Chlorophenoxy)propanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1266)

To a solution of 150 mg (0.748 mmol) of 2-(2-chlorophenoxy)propanoic acid in 3 ml of dehydrated dichloromethane, 0.080 ml (0.93 mmol) of oxalyl chloride and 0.004 ml (0.05 mmol) of DMF were added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 129 mg (0.341 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.300 ml (1.72 mmol) of DIPEA in 3 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 3 hours. Subsequently, 0.200 ml (1.84 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then reacted with stirring at room temperature for 16 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain a solid. The obtained solid was subjected again to silica gel column chromatography (DNH silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 16 mg of the title compound (yield: 10%) as a white solid.

Mass spectrum (CI, m/z): 489 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.32 & 11.92 (br s, total 1H), 9.80-9.54 (m, 1H), 7.45-7.38 (m, 1H), 7.29-7.20 (m, 1H), 6.96-6.89 (m, 1H), 6.89-6.83 (m, 1H), 5.01 (q, J=6.5 Hz, 1H), 4.92-4.74 (m, 1H), 4.72-4.52 (m, 1H), 2.58-2.37 (m, 2H), 2.27-2.10 (m, 2H), 1.93-1.71 (m, 2H), 1.71-1.55 (m, 6H), 1.51 (d, J=6.5 Hz, 3H), 0.06 (s, 9H).

Example 76 N-{5-[2-(Cyclohexyloxy)propanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1255)

To a solution of 120 mg (0.697 mmol) of 2-(cyclohexyloxy)propanoic acid [purchased from Enamine Ltd.] in 3 ml of dehydrated dichloromethane, 0.080 ml (0.93 mmol) of oxalyl chloride and 0.005 ml (0.07 mmol) of DMF were added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 129 mg (0.341 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.300 ml (1.72 mmol) of DIPEA in 3 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 2 hours. Subsequently, 0.200 ml (1.84 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then reacted with stirring at room temperature for 16 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 37 mg of the title compound (yield: 24%) as a white solid.

Mass spectrum (CI, m/z): 461 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.39-11.73 (m, 1H), 9.63 (br s, 1H), 4.78-4.55 (m, 2H), 4.23 (q, J=6.5 Hz, 1H), 3.41-3.26 (m, 1H), 2.58-2.37 (m, 2H), 2.25-2.12 (m, 2H), 1.90-1.72 (m, 4H), 1.71-1.55 (m, 8H), 1.50-1.39 (m, 1H), 1.28-1.05 (m, 8H), 0.07 (s, 9H).

Example 77 N-{5-[2-(3-Chlorophenoxy)propanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1268)

To a solution of 150 mg (0.748 mmol) of 2-(3-chlorophenoxy)propanoic acid [purchased from Combi-Blocks Inc.] in 3 ml of dehydrated dichloromethane, 0.080 ml (0.93 mmol) of oxalyl chloride and 0.005 ml (0.07 mmol) of DMF were added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 129 mg (0.341 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.300 ml (1.72 mmol) of DIPEA in 3 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 2 hours. Subsequently, 0.200 ml (1.84 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then reacted with stirring at room temperature for 16 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure. The obtained solid was subjected again to silica gel column chromatography (DNH silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 30 mg of the title compound (yield: 18%) as a white solid.

Mass spectrum (CI, m/z): 489 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.32 & 11.93 (br s, total 1H), 9.79-9.56 (m, 1H), 7.29 (t, J=8.3 Hz, 1H), 7.00-6.94 (m, 1H), 6.86 (t, J=2.1 Hz, 1H), 6.83-6.77 (m, 1H), 5.00 (q, J=6.4 Hz, 1H), 4.90-4.73 (m, 1H), 4.71-4.51 (m, 1H), 2.57-2.37 (m, 2H), 2.27-2.10 (m, 2H), 1.92-1.71 (m, 2H), 1.70-1.53 (m, 6H), 1.47 (d, J=6.4 Hz, 3H), 0.06 (s, 9H).

Example 78 N-[5-(2-Methoxypropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1241)

To a solution of 65.0 mg (0.624 mmol) of 2-methoxypropanoic acid [purchased from Combi-Blocks Inc.] in 3 ml of dehydrated dichloromethane, 0.200 ml (1.15 mmol) of DIPEA and 220 mg (0.514 mmol) of (1-cyano-2-ethoxy-2-oxoethylideneaminooxy)dimethylaminomorpholinocarbenium hexafluorophosphate [COMU (trade name)] were added in this order with stirring at 0° C. in an argon atmosphere and then stirred at the same temperature as above for 15 minutes. Subsequently, 129 mg (0.341 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 was added at 0° C. and stirred at room temperature for 16 hours. Subsequently, 0.220 ml (2.02 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then reacted with stirring at room temperature for 4 hours.

The reaction solution was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 61 mg of the title compound (yield: 46%) as a white solid.

Mass spectrum (CI, m/z): 393 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.28 & 11.86 (br s, total 1H), 9.80-9.53 (m, 1H), 4.82-4.44 (m, 2H), 4.06 (q, J=6.4 Hz, 1H), 3.20 (s, 3H), 2.57-2.37 (m, 2H), 2.29-2.10 (m, 2H), 1.93-1.55 (m, 8H), 1.21 (d, J=6.4 Hz, 3H), 0.08 (s, 9H).

Example 79 N-[5-(3-Methoxy-2-phenoxypropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1348)

To a solution of 116 mg of 3-methoxy-2-phenoxypropanoic acid (containing impurities) synthesized in the similar manner as in Reference Example 63 in 3 ml of dehydrated dichloromethane, 0.004 ml (0.05 mmol) of DMF and 0.070 ml (0.82 mmol) of oxalyl chloride were added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 124 mg (0.329 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.300 ml (1.72 mmol) of DIPEA in 3 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 2 hours. Subsequently, 0.200 ml (1.84 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then reacted with stirring at room temperature for 16 hours.

The reaction solution was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 75 mg of the title compound (yield: 47%) as a white solid.

Mass spectrum (CI, m/z): 485 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.32 & 11.94 (br s, total 1H), 9.85-9.57 (m, 1H), 7.34-7.21 (m, 2H), 6.97-6.89 (m, 1H), 6.88-6.78 (m, 2H), 4.98-4.79 (m, 2H), 4.78-4.59 (m, 1H), 3.83-3.68 (m, 2H), 3.34 (s, 3H), 2.58-2.37 (m, 2H), 2.28-2.10 (m, 2H), 1.92-1.71 (m, 2H), 1.69-1.49 (m, 6H), 0.08 (s, 9H).

Example 80 N-{6,6-Dimethyl-5-[2-(pyridin-3-yloxy)propanoyl]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1274)

To a solution of 114 mg (0.682 mmol) of 2-(pyridin-3-yloxy)propanoic acid [purchased from Enamine Ltd.] in 3 ml of dehydrated dichloromethane, 0.200 ml (1.15 mmol) of DIPEA and 250 mg (0.584 mmol) of (1-cyano-2-ethoxy-2-oxoethylideneaminooxy)dimethylaminomorpholinocarbenium hexafluorophosphate [COMU (trade name)] were added in this order with stirring at 0° C. in an argon atmosphere and then stirred at the same temperature as above for 15 minutes. Subsequently, 172 mg (0.454 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 was added at 0° C. and stirred at room temperature for 16 hours. Subsequently, 0.250 ml (2.30 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then reacted with stirring at room temperature for 4 hours.

The reaction solution was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 89 mg of the title compound (yield: 43%) as a white solid.

Mass spectrum (CI, m/z): 456 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.32 & 11.88 (s, total 1H), 9.76-9.60 (m, 1H), 8.24-8.17 (m, 1H), 8.17-8.09 (m, 1H), 7.33-7.27 (m, 1H), 7.25-7.20 (m, 1H), 5.06 (q, J=6.3 Hz, 1H), 4.93-4.79 (m, 1H), 4.70-4.54 (m, 1H), 2.57-2.38 (m, 2H), 2.27-2.13 (m, 2H), 1.91-1.71 (m, 2H), 1.69-1.54 (m, 6H), 1.50 (d, J=6.3 Hz, 3H), 0.13-0.02 (m, 9H).

Example 81 N-{5-[3-(Dimethylamino)-2-phenoxypropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1372)

To a solution of 70.0 mg (0.335 mmol) of 3-(dimethylamino)-2-phenoxypropanoic acid synthesized in the similar manner as in Reference Example 66 in 3 ml of dehydrated DMF, 0.150 ml (0.861 mmol) of DIPEA and 200 mg (0.467 mmol) of (1-cyano-2-ethoxy-2-oxoethylideneaminooxy)dimethylaminomorpholinocarbenium hexafluorophosphate [COMU (trade name)] were added in this order with stirring at 0° C. in an argon atmosphere and then stirred at the same temperature as above for 15 minutes. Subsequently, 115 mg (0.304 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 was added at 0° C. and stirred at room temperature for 3 hours. Subsequently, 0.200 ml (1.84 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then reacted with stirring at room temperature for 16 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: 1,2-dichloroethane:methanol=100:0 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 57 mg of the title compound (yield: 38%) as a white solid.

Mass spectrum (CI, m/z): 498 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.48-11.69 (m, 1H), 9.67 (br s, 1H), 7.32-7.23 (m, 2H), 6.96-6.88 (m, 1H), 6.84-6.77 (m, 2H), 4.87 (br d, J=12.0 Hz, 1H), 4.81 (dd, J=4.5, 6.6 Hz, 1H), 4.66 (br d, J=12.0 Hz, 1H), 2.82-2.70 (m, 2H), 2.57-2.39 (m, 2H), 2.26 (s, 6H), 2.24-2.12 (m, 2H), 1.89-1.73 (m, 2H), 1.62 (s, 3H), 1.61 (s, 3H), 0.07 (s, 9H).

Example 82 N-[6,6-Dimethyl-5-(2-phenoxy-2-phenylacetyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1211)

To a solution of 140 mg (0.613 mmol) of 2-phenoxy-2-phenylacetic acid [purchased from Enamine Ltd.] in 3 ml of dehydrated dichloromethane, 0.080 ml (0.93 mmol) of oxalyl chloride and 0.005 ml (0.07 mmol) of DMF were added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 129 mg (0.341 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.300 ml (1.72 mmol) of DIPEA in 3 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 3 hours. Subsequently, 0.200 ml (1.84 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then reacted with stirring at room temperature for 16 hours.

The reaction solution was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 94 mg of the title compound (yield: 53%) as a white solid.

Mass spectrum (CI, m/z): 517 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.30 & 11.91 (br s, total 1H), 9.57 (br s, 1H), 7.57-7.50 (m, 2H), 7.48-7.36 (m, 3H), 7.31-7.23 (m, 2H), 6.97-6.88 (m, 3H), 5.91 (s, 1H), 4.98-4.72 (m, 1H), 4.40-4.21 (m, 1H), 2.48-2.35 (m, 2H), 2.27-2.08 (m, 2H), 1.91-1.73 (m, 2H), 1.67 (s, 3H), 1.60 (s, 3H), 0.04 (s, 9H).

Example 83 N-{5-[3-(3,3-Difluoropyrrolidin-1-yl)-2-phenoxypropanoyl]-6,6-dimeth yl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1378)

To a solution of 170 mg of 3-(3,3-difluoropyrrolidin-1-yl)-2-phenoxypropanoic acid (containing impurities) synthesized in the similar manner as in Reference Example 69 in 3 ml of dehydrated DMF, 0.250 ml (1.44 mmol) of DIPEA and 300 mg (0.700 mmol) of (1-cyano-2-ethoxy-2-oxoethylideneaminooxy)dimethylaminomorpholinocarbenium hexafluorophosphate [COMU (trade name)] were added in this order with stirring at 0° C. in an argon atmosphere and then stirred at the same temperature as above for 15 minutes. Subsequently, 129 mg (0.341 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 was added at 0° C. and stirred at room temperature for 16 hours. Subsequently, 0.200 ml (1.84 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then reacted with stirring at room temperature for 64 hours.

The reaction solution was subjected to silica gel column chromatography (elution solvent: 1,2-dichloroethane:methanol=100:0 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected to preparative HPLC (column: X-Bridge (trade name) ODS, elution solvent: acetonitrile:1 mM aqueous potassium dihydrogen phosphate solution=50:50 (V/V)), and ethyl acetate and water were added to a fraction containing the compound of interest, then an organic layer and an aqueous layer were separated. The obtained organic layer was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 49 mg of the title compound (yield: 26%) as a white solid.

Mass spectrum (CI, m/z): 560 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.32 & 11.94 (br s, total 1H), 9.84-9.59 (m, 1H), 7.32-7.23 (m, 2H), 6.97-6.89 (m, 1H), 6.85-6.78 (m, 2H), 4.97-4.80 (m, 2H), 4.74-4.57 (m, 1H), 3.14-2.80 (m, 6H), 2.58-2.37 (m, 2H), 2.29-2.10 (m, 4H), 1.92-1.72 (m, 2H), 1.70-1.52 (m, 6H), 0.14-0.03 (m, 9H).

Example 84 N-[5-(3-Hydroxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-632)

To a solution of 139 mg (0.540 mmol) of 3-(benzyloxy)-2-phenylpropanoic acid synthesized according to the method described in Tetrahedron Lett., 2002 (43), 9691-9693] in 3 ml of dehydrated DMF, 0.18 ml (1.0 mmol) of DIPEA and 233 mg (0.544 mmol) of (1-cyano-2-ethoxy-2-oxoethylideneaminooxy)dimethylaminomorpholinocarbenium hexafluorophosphate [COMU (trade name)] were added in this order at 0° C. in a nitrogen atmosphere and then stirred for 15 minutes with the temperature unchanged. Subsequently, 158 mg (0.418 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate synthesized in the similar manner as in Reference Example 5 was added at 0° C. and then stirred at room temperature for 3.5 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred, followed by extraction with ethyl acetate three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure to obtain a concentration residue.

To a solution of the obtained concentration residue in 4 ml of THF, 0.25 ml (1.8 mmol) of triethylamine and 0.10 ml (1.7 mmol) of 2-aminoethanol were added in this order at room temperature in a nitrogen atmosphere and then stirred for 1.5 hours with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=70:30 to 50:50 (V/V)), subsequently concentrated under reduced pressure, and dried under reduced pressure to obtain a concentration residue.

To a solution of the obtained concentration residue in 2 ml of ethanol, 25.4 mg of 20% palladium hydroxide/carbon [containing 50 wt % water] was added at room temperature in a nitrogen atmosphere and then, after replacement with a hydrogen atmosphere under reduced pressure, stirred at room temperature for 1.5 hours. The inside of the reaction container was replaced with a nitrogen atmosphere under reduced pressure, and subsequently, 68.3 mg of 20% palladium hydroxide/carbon [containing 50 wt % water] was added at room temperature and then, after replacement with a hydrogen atmosphere again under reduced pressure, stirred at room temperature for 3.5 hours.

After the completion of the reaction, the inside of the reaction container was replaced with a nitrogen atmosphere under reduced pressure. The reaction solution was filtered using a celite filter, subsequently the removed solid was washed with ethanol, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=70:30 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 104 mg of the title compound (yield: 55% [2 steps]) as a white solid.

Mass spectrum (EI, m/z): 454 [M]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.45-11.70 (m, 1H), 9.58 (br s, 1H), 7.35-7.20 (m, 5H), 4.81-4.64 (m, 2H), 4.23 (d, J=12.0 Hz, 1H), 3.98-3.89 (m, 1H), 3.84 (dd, J=5.4, 8.2 Hz, 1H), 3.52-3.44 (m, 1H), 2.58-2.37 (m, 2H), 2.24-2.12 (m, 2H), 1.87-1.73 (m, 2H), 1.69 (s, 3H), 1.58 (s, 3H), 0.05 (s, 9H).

Example 85 (S)—N-[5-(3-Hydroxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-633)

To a solution of 139 mg (0.256 mmol) of (S)—N-{5-[3-(benzyloxy)-2-phenylpropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide synthesized in the similar manner as in Reference Example 70 in 2 ml of ethanol, 58.4 mg of 20% palladium hydroxide/carbon [containing 50 wt % water] was added at room temperature in a nitrogen atmosphere and then, after replacement with a hydrogen atmosphere under reduced pressure, stirred at room temperature for 3 hours.

After the completion of the reaction, the inside of the reaction container was replaced with a nitrogen atmosphere under reduced pressure. The reaction solution was filtered using a celite filter, subsequently the removed solid was washed with ethyl acetate, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=85:15 to 35:65 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 55 mg of the title compound (yield: 47%) as a white solid.

Mass spectrum (CI, m/z): 455 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.24 & 11.85 (br s, total 1H), 9.73-9.44 (m, 1H), 7.35-7.20 (m, 5H), 4.81-4.63 (m, 2H), 4.33-4.11 (m, 1H), 3.98-3.89 (m, 1H), 3.88-3.80 (m, 1H), 3.52-3.44 (m, 1H), 2.60-2.36 (m, 2H), 2.26-2.10 (m, 2H), 1.89-1.64 (m, 5H), 1.58 (br s, 3H), 0.05 (s, 9H).

Example 86 (R)—N-{5-[3-(Benzyloxy)-2-phenylpropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1221)

To a solution of 1.22 g (4.76 mmol) of (R)-3-(benzyloxy)-2-phenylpropanoic acid [synthesized according to the method described in Tetrahedron Lett., 2002, 43, 9691-9693] in 20 ml of dehydrated dichloromethane, 0.55 ml (6.4 mmol) of oxalyl chloride and 0.030 ml (0.39 mmol) of dehydrated DMF were added in this order at 0° C. in a nitrogen atmosphere and then stirred for 2 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 903 mg (2.39 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 1.70 ml (9.76 mmol) of DIPEA in 15 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 5 ml of dehydrated dichloromethane was added at 0° C. in a nitrogen atmosphere and then stirred for 2 hours with the temperature unchanged. Subsequently, 1.0 ml (9.2 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at 0° C. and then stirred at room temperature for 1.5 hours.

After the completion of the reaction, the reaction solution diluted with dichloromethane was washed with a 5% aqueous potassium bisulfate solution and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with dichloromethane twice, and then, all of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=85:15 to 50:50 (V/V)), and some fractions containing the compound of interest at high purity were concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 43 mg of the title compound (yield: 3%) as a white solid. Also, the remaining fractions containing the compound of interest obtained by silica gel column chromatography were concentrated under reduced pressure and dried under reduced pressure to obtain 1.10 g of the title compound (yield: 85%) as a pale yellow foam.

Mass spectrum (CI, m/z): 545 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.25 & 11.85 (s, total 1H), 9.65-9.47 (m, 1H), 7.38-7.20 (m, 10H), 4.79-4.62 (m, 1H), 4.52 (d, J=12.6 Hz, 1H), 4.47 (d, J=12.6 Hz, 1H), 4.31-4.15 (m, 1H), 4.07-3.94 (m, 2H), 3.57-3.47 (m, 1H), 2.57-2.36 (m, 2H), 2.25-2.09 (m, 2H), 1.89-1.64 (m, 5H), 1.63-1.50 (m, 3H), 0.09-0.02 (m, 9H).

Example 87 (R)—N-[5-(3-Hydroxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1215)

To a solution of 1.10 g (2.02 mmol) of (R)—N-{5-[3-(benzyloxy)-2-phenylpropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide synthesized in the similar manner as in Example 86 in 15 ml of ethanol, 326 mg of 20% palladium hydroxide/carbon [containing 50 wt % water] was added at room temperature in a nitrogen atmosphere and then, after replacement with a hydrogen atmosphere under reduced pressure, stirred at room temperature for 3.5 hours.

After the completion of the reaction, the inside of the reaction container was replaced with a nitrogen atmosphere under reduced pressure. The reaction solution was filtered using a celite filter, subsequently the removed solid was washed with ethyl acetate, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=70:30 to 10:90 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel column chromatography (elution solvent: dichloromethane:methanol=100:0 to 96:4 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 708 mg of the title compound (yield: 77%) as a white solid.

Mass spectrum (CI, m/z): 455 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.25 & 11.82 (s, total 1H), 9.66-9.47 (m, 1H), 7.36-7.20 (m, 5H), 4.83-4.62 (m, 2H), 4.32-4.13 (m, 1H), 3.99-3.90 (m, 1H), 3.89-3.79 (m, 1H), 3.53-3.42 (m, 1H), 2.57-2.35 (m, 2H), 2.25-2.09 (m, 2H), 1.91-1.64 (m, 5H), 1.63-1.52 (m, 3H), 0.13-0.01 (m, 9H).

Example 88 (R)—N-[5-(2-Methoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1175)

To a solution of 263 mg (1.58 mmol) of (R)-2-methoxy-2-phenylacetic acid in 5 ml of dehydrated dichloromethane, 0.24 ml (2.8 mmol) of oxalyl chloride and 0.025 ml (0.32 mmol) of DMF were added in this order at 0° C. in an argon atmosphere and then stirred for 3 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure at room temperature to obtain a concentration residue.

To a solution of 300 mg (0.793 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.55 ml (3.2 mmol) of DIPEA in 5 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 3 ml of dehydrated dichloromethane was added dropwise at 0° C. in an argon atmosphere and then stirred at room temperature for 15 hours. Subsequently, 0.37 ml (4.0 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then stirred for 3 hours with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with ethyl acetate. All of the obtained organic layers were washed with a saturated aqueous solution of ammonium chloride and a saturated aqueous solution of sodium chloride in this order, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=50:50 to 35:65 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 224 mg of the title compound (yield: 62%) as a white solid.

Mass spectrum (CI, m/z): 455 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.26 & 11.86 (br s, total 1H), 9.71-9.47 (m, 1H), 7.44-7.27 (m, 5H), 4.96 (s, 1H), 4.74-4.52 (m, 1H), 4.39-4.21 (m, 1H), 3.31 (s, 3H), 2.48-2.36 (m, 2H), 2.26-2.07 (m, 2H), 1.92-1.53 (m, 8H), 0.05 (s, 9H).

Example 89 (S)—N-[5-(2-Methoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1176)

To a solution of 263 mg (1.58 mmol) of (S)-2-methoxy-2-phenylacetic acid in 5 ml of dehydrated dichloromethane, 0.24 ml (2.8 mmol) of oxalyl chloride and 0.025 ml (0.32 mmol) of DMF were added in this order at 0° C. in an argon atmosphere and then stirred for 3 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure at room temperature to obtain a concentration residue.

To a solution of 300 mg (0.793 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.55 ml (3.2 mmol) of DIPEA in 5 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 3 ml of dehydrated dichloromethane was added dropwise at 0° C. in an argon atmosphere and then stirred at room temperature for 15 hours. Subsequently, 0.37 ml (4.0 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then stirred for 3 hours with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with ethyl acetate. All of the obtained organic layers were washed with a saturated aqueous solution of ammonium chloride and a saturated aqueous solution of sodium chloride in this order, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=50:50 to 35:65 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved by adding ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 206 mg of the title compound (yield: 57%) as a white solid.

Mass spectrum (CI, m/z): 455 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.26 & 11.86 (br s, total 1H), 9.71-9.45 (m, 1H), 7.46-7.26 (m, 5H), 4.96 (s, 1H), 4.73-4.53 (m, 1H), 4.30 (br d, J=12.3 Hz, 1H), 3.31 (s, 3H), 2.47-2.36 (m, 2H), 2.24-2.11 (m, 2H), 1.89-1.53 (m, 8H), 0.05 (s, 9H).

Example 90 N-[5-(3-Methoxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-634)

To a solution of 212 mg (1.18 mmol) of 3-methoxy-2-phenylpropanoic acid synthesized in the similar manner as in Reference Example 72 in 6 ml of dehydrated dichloromethane, 0.14 ml (1.6 mmol) of oxalyl chloride and 0.0060 ml (0.077 mmol) of dehydrated DMF were added in this order at 0° C. in a nitrogen atmosphere and then stirred for 2.5 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 156 mg (0.413 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.36 ml (2.1 mmol) of DIPEA in 3 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added at 0° C. in a nitrogen atmosphere and then stirred for 1.5 hours with the temperature unchanged. Subsequently, 0.23 ml (2.1 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at 0° C. and then stirred at room temperature for 2 hours.

After the completion of the reaction, the reaction solution diluted with dichloromethane was washed with a 5% aqueous potassium bisulfate solution, and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with dichloromethane twice, and then, all of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=70:30 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel column chromatography (elution solvent: dichloromethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected to preparative HPLC (column: X-Bridge (trade name) ODS, elution solvent: acetonitrile:1 mM aqueous dipotassium hydrogen phosphate solution=40:60 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, and acetonitrile was distilled off. The obtained concentration residue was subjected to extraction with ethyl acetate three times, and then, all of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, subsequently dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 101 mg of the title compound (yield: 52%) as a white solid.

Mass spectrum (CI, m/z): 469 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.50-11.61 (m, 1H), 9.57 (br s, 1H), 7.36-7.22 (m, 5H), 4.70 (d, J=12.3 Hz, 1H), 4.22 (d, J=12.3 Hz, 1H), 3.99-3.92 (m, 1H), 3.90-3.83 (m, 1H), 3.40 (dd, J=5.7, 8.8 Hz, 1H), 3.23 (s, 3H), 2.57-2.37 (m, 2H), 2.22-2.12 (m, 2H), 1.86-1.74 (m, 2H), 1.68 (s, 3H), 1.57 (s, 3H), 0.05 (s, 9H).

Example 91 N-[5-(4-Methoxy-2-phenylbutanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1224)

To a solution of 154 mg (0.793 mmol) of 4-methoxy-2-phenylbutanoic acid synthesized in the similar manner as in Reference Example 74 in 3 ml of dehydrated dichloromethane, 0.14 ml (1.6 mmol) of oxalyl chloride and 0.0092 ml (0.12 mmol) of DMF were added in this order at 0° C. in an argon atmosphere and then stirred for 1 hour with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure at room temperature to obtain a concentration residue.

To a solution of 150 mg (0.396 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.28 ml (1.6 mmol) of DIPEA in 3 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 3 ml of dehydrated dichloromethane was added dropwise at 0° C. in an argon atmosphere and then stirred at room temperature for 3 hours. Subsequently, 0.185 ml (1.98 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then stirred for 14 hours with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with ethyl acetate. All of the obtained organic layers were washed with a saturated aqueous solution of ammonium chloride and a saturated aqueous solution of sodium chloride in this order, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 40:60 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected to preparative HPLC (column: XSelect (trade name) HSS C18, elution solvent: acetonitrile:1 mM aqueous potassium dihydrogen phosphate solution=50:50 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, and acetonitrile was distilled off. The obtained concentration residue was subjected to extraction with ethyl acetate, and all of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was dissolved by adding ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 78 mg of the title compound (yield: 41%) as a white solid.

Mass spectrum (CI, m/z): 483 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.24 & 11.95 (br s, total 1H), 9.78-9.46 (m, 1H), 7.39-7.18 (m, 5H), 4.79-4.57 (m, 1H), 4.24 (br d, J=12.2 Hz, 1H), 3.92-3.75 (m, 1H), 3.29-3.21 (m, 2H), 3.20 (s, 3H), 2.59-2.37 (m, 2H), 2.25-2.11 (m, 3H), 1.88-1.62 (m, 6H), 1.57 (br s, 3H), 0.05 (s, 9H).

Example 92 (S)—N-[5-(3-Hydroxy-2-phenylpropanoyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclopropanecarboxamide (Compound No. III-592)

To a solution of 45.8 mg (0.0864 mmol) of (S)—N-{5-[3-(benzyloxy)-2-phenylpropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclopropanecarboxamide synthesized in the similar manner as in Reference Example 75 in 1 ml of ethanol, 13.6 mg of 20% palladium hydroxide/carbon [containing 50 wt % water] was added at room temperature in a nitrogen atmosphere and then, after replacement with a hydrogen atmosphere under reduced pressure, stirred at room temperature for 2.5 hours.

After the completion of the reaction, the inside of the reaction container was replaced with a nitrogen atmosphere under reduced pressure. The reaction solution was filtered using a celite filter, subsequently the removed solid was washed with ethyl acetate, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=70:30 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel column chromatography (elution solvent: dichloromethane:methanol=99:1 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 19 mg of the title compound (yield: 50%) as a white solid.

Mass spectrum (CI, m/z): 441 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.25 & 11.96 (br s, total 1H), 9.98-9.65 (m, 1H), 7.37-7.19 (m, 5H), 4.80-4.58 (m, 2H), 4.33-4.10 (m, 1H), 3.98-3.88 (m, 1H), 3.88-3.80 (m, 1H), 3.52-3.43 (m, 1H), 1.68 (br s, 3H), 1.57 (br s, 3H), 1.05-0.91 (m, 2H), 0.80-0.56 (m, 2H), 0.01 (s, 9H).

Example 93 (R)—N-[5-(2-Methoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclopropanecarboxamide (Compound No. III-1059)

To a solution of 182 mg (1.10 mmol) of (R)-2-methoxy-2-phenylacetic acid in 5 ml of dehydrated dichloromethane, 0.165 ml (1.92 mmol) of oxalyl chloride and 0.017 ml (0.22 mmol) of DMF were added in this order at 0° C. in an argon atmosphere and then stirred for 1 hour with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure at room temperature to obtain a concentration residue.

To a solution of 200 mg (0.549 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 46 and 0.38 ml (2.2 mmol) of DIPEA in 5 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 3 ml of dehydrated dichloromethane was added dropwise at 0° C. in an argon atmosphere and then stirred at room temperature for 1.5 hours. Subsequently, 0.26 ml (2.7 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then stirred for 1 hour with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with ethyl acetate. All of the obtained organic layers were washed with a saturated aqueous solution of ammonium chloride and a saturated aqueous solution of sodium chloride in this order, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=70:30 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel column chromatography (elution solvent: 1,2-dichloroethane:methanol=97:3 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 191 mg of the title compound (yield: 79%) as a white solid.

Mass spectrum (CI, m/z): 441 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.38-11.88 (m, 1H), 9.97-9.65 (m, 1H), 7.45-7.27 (m, 5H), 4.96 (s, 1H), 4.71-4.49 (m, 1H), 4.29 (br d, J=12.8 Hz, 1H), 3.31 (s, 3H), 1.68 (br s, 3H), 1.59 (s, 3H), 1.05-0.91 (m, 2H), 0.78-0.58 (m, 2H), 0.01 (s, 9H).

Example 94 (R)—N-{5-[2-(Difluoromethoxy)-2-phenylacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1180)

To a solution of 1.01 g (4.17 mmol) of (R)-benzyl 2-hydroxy-2-phenylacetate and 158 mg (0.83 mmol) of copper(I) iodide in 15 ml of acetonitrile, a solution of 2.2 ml (17 mmol) of 2,2-difluoro-2-(fluorosulfonyl)acetic acid in 20 ml of acetonitrile was dividedly added (2 ml each) every 5 minutes at 60° C. in an argon atmosphere and stirred for 2 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution allowed to cool to room temperature was concentrated under reduced pressure and diluted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 70:30 (V/V)), and subsequently, a fraction containing the compound of interest was concentrated under reduced pressure to obtain 0.67 g of a concentration residue as a colorless oil.

To a solution of 0.67 g of the obtained concentration residue in 20 ml of methanol, 70 mg of palladium/carbon (ASCA2 (trade name), manufactured by N.E. Chemcat Corp., containing 54% water) was added in an argon atmosphere and then, after replacement with a hydrogen atmosphere under reduced pressure, stirred at room temperature for 2 hours.

After the completion of the reaction, replacement with a nitrogen atmosphere was performed, the reaction solution was filtered through celite, the solid component was washed with methanol, and then, the filtrate was concentrated under reduced pressure to obtain 0.42 g of a concentration residue as a pale yellow solid.

To a solution of 115 mg of the obtained concentration residue in 3 ml of dehydrated dichloromethane, 0.072 ml (0.82 mmol) of oxalyl chloride and 0.010 ml (0.13 mmol) of dehydrated DMF were added in this order at room temperature in an argon atmosphere and then stirred for 15 minutes with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 103 mg (0.273 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.24 ml (1.4 mmol) of DIPEA in 3 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added at room temperature in an argon atmosphere and then stirred for 3.5 hours with the temperature unchanged. Subsequently, 0.15 ml (1.4 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at room temperature and then stirred at room temperature for 1 hour.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in this order, dried by adding anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=50:50 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, and n-hexane was added. The deposited solid was collected by filtration and dried under reduced pressure to obtain 48.1 mg of the title compound (yield: 36%) as a white solid.

Mass spectrum (CI, m/z): 491 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.30 & 11.86 (br s, total 1H), 9.67-9.51 (m, 1H), 7.48-7.37 (m, 5H), 6.83 (t, J=76.0 Hz, 1H), 5.78 (s, 1H), 4.83-4.61 (m, 1H), 4.24-4.07 (m, 1H), 2.56-2.35 (m, 2H), 2.24-2.10 (m, 2H), 1.91-1.50 (m, 8H), 0.04 (s, 9H).

Example 95 (R)—N-[5-(2-Ethoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1188)

To a solution of 128 mg (0.710 mmol) of (R)-2-ethoxy-2-phenylacetic acid obtained in the similar manner as in Reference Example 77 in 3 ml of dehydrated dichloromethane, 0.090 ml (1.0 mmol) of oxalyl chloride and 0.010 ml (0.13 mmol) of dehydrated DMF were added in this order at 0° C. in an argon atmosphere and then stirred for 1 hour with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 112 mg (0.295 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.30 ml (1.7 mmol) of DIPEA in 3 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added at 0° C. in an argon atmosphere and then stirred for 30 minutes with the temperature unchanged. Subsequently, 0.11 ml (1.01 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at 0° C. and then stirred at room temperature for 1 hour.

After the completion of the reaction, water was added, followed by extraction with ethyl acetate. The organic layer was washed with a 5% aqueous potassium bisulfate solution and a saturated aqueous solution of sodium chloride in this order, dried by adding anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=50:50 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, n-hexane was added, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 69.7 mg of the title compound (yield: 50%) as a white solid.

Mass spectrum (CI, m/z): 469 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.26 & 11.85 (br s, total 1H), 9.67-9.48 (m, 1H), 7.43-7.27 (m, 5H), 5.04 (s, 1H), 4.73-4.47 (m, 1H), 4.44-4.24 (m, 1H), 3.62-3.40 (m, 2H), 2.58-2.36 (m, 2H), 2.25-2.10 (m, 2H), 1.90-1.53 (m, 8H), 1.14 (t, J=7.0 Hz, 3H), 0.05 (s, 9H).

Example 96 (R)-1-(Ethyldimethylsilyl)-N-[5-(2-methoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]cyclobutanecarboxamide (Compound No. IV-1178)

To a solution of 107 mg (0.646 mmol) of (R)-2-methoxy-2-phenylacetic acid in 2 ml of dehydrated dichloromethane, 0.080 ml (0.93 mmol) of oxalyl chloride and 0.0050 ml (0.065 mmol) of dehydrated DMF were added in this order at 0° C. in a nitrogen atmosphere and then stirred for 3 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 117 mg (0.299 mmol) of ethyl 3-[1-(ethyldimethylsilyl)cyclobutanecarboxamido]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 12 and 0.21 ml (1.2 mmol) of DIPEA in 1 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added at 0° C. in a nitrogen atmosphere and then stirred for 2.5 hours with the temperature unchanged. Subsequently, 0.16 ml (1.5 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at 0° C. and then stirred at room temperature for 1.5 hours.

After the completion of the reaction, the reaction solution diluted with dichloromethane was washed with a 5% aqueous potassium bisulfate solution and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with dichloromethane twice, and then, all of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=80:20 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 115 mg of the title compound (yield: 82%) as a white solid.

Mass spectrum (CI, m/z): 469 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.26 & 11.84 (s, total 1H), 9.67-9.48 (m, 1H), 7.42-7.27 (m, 5H), 4.95 (s, 1H), 4.71-4.52 (m, 1H), 4.35-4.23 (m, 1H), 3.30 (s, 3H), 2.56-2.37 (m, 2H), 2.26-2.11 (m, 2H), 1.90-1.52 (m, 8H), 0.88 (t, J=7.8 Hz, 3H), 0.53 (q, J=7.8 Hz, 2H), 0.09-0.01 (m, 6H).

Example 97 (R)—N-[5-(2-Cyclopropoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1208)

To a solution of 140 mg (0.728 mmol) of (R)-2-cyclopropoxy-2-phenylacetic acid synthesized in the similar manner as in Reference Example 86 in 2 ml of dehydrated dichloromethane, 0.006 ml (0.08 mmol) of DMF and 0.083 ml (0.95 mmol) of oxalyl chloride were added with stirring at 0° C. in an argon atmosphere and stirred at room temperature for 1.5 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 150 mg (0.396 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydro pyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.350 ml (2.00 mmol) of DIPEA in 2 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 3 ml of dehydrated dichloromethane was added dropwise with stirring at 0° C. in an argon atmosphere and stirred at room temperature for 2 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with water, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 70:30 (V/V)), subsequently concentrated under reduced pressure, and dried under reduced pressure to obtain a concentration residue.

To a solution of the obtained concentration residue in 2 ml of dehydrated dichloromethane, 0.130 ml (1.19 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature in an argon atmosphere and then stirred at room temperature for 16 hours.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate and then added to n-hexane, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 80 mg of the title compound (yield: 42%) as a white solid.

Mass spectrum (CI, m/z): 481 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.37-11.83 (m, 1H), 9.59 (br s, 1H), 7.42-7.28 (m, 5H), 5.10 (s, 1H), 4.73-4.54 (m, 1H), 4.35 (d, J=12.4 Hz, 1H), 3.40 (tt, J=3.0, 6.1 Hz, 1H), 2.59-2.37 (m, 2H), 2.24-2.12 (m, 2H), 1.90-1.74 (m, 2H), 1.70 (s, 3H), 1.61 (s, 3H), 0.69-0.53 (m, 2H), 0.51-0.39 (m, 2H), 0.05 (s, 9H).

Example 98 (R)—N-[5-(2-Isopropoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1204)

To a solution of 165 mg (0.849 mmol) of (R)-2-isopropoxy-2-phenylacetic acid synthesized in the similar manner as in Reference Example 87 in 2 ml of dehydrated dichloromethane, 0.10 ml (1.2 mmol) of oxalyl chloride and 0.0050 ml (0.065 mmol) of dehydrated DMF were added in this order at 0° C. in an argon atmosphere and then stirred for 2.5 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure and dried under reduced pressure to obtain a concentration residue.

To a solution of 128 mg (0.338 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.30 ml (1.7 mmol) of DIPEA in 1 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added at 0° C. in an argon atmosphere and then stirred for 1.5 hours with the temperature unchanged.

After the completion of the reaction, ethyl acetate and a saturated aqueous solution of sodium bicarbonate were added to the reaction solution and stirred. After separation into an aqueous layer and an organic layer, the aqueous layer was subjected to extraction with ethyl acetate twice. All of the organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=80:20 to 60:40 (V/V)), subsequently concentrated under reduced pressure, and dried under reduced pressure to obtain a concentration residue.

To a solution of the obtained concentration residue in 2 ml of THF, 0.15 ml (1.4 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature in an argon atmosphere and then stirred at room temperature for 2 hours.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with ethyl acetate three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=80:20 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 135 mg of the title compound (yield: 83%) as a white solid.

Mass spectrum (CI, m/z): 483 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.40-11.82 (m, 1H), 9.75-9.42 (m, 1H), 7.40-7.27 (m, 5H), 5.11 (s, 1H), 4.65-4.38 (m, 2H), 3.68 (spt, J=6.0 Hz, 1H), 2.47-2.35 (m, 2H), 2.23-2.09 (m, 2H), 1.87-1.71 (m, 2H), 1.67 (s, 3H), 1.61 (s, 3H), 1.16 (d, J=6.0 Hz, 3H), 1.13 (d, J=6.0 Hz, 3H), 0.04 (s, 9H).

Example 99 (R)—N-{6,6-Dimethyl-5-[2-phenyl-2-(trifluoromethoxy)acetyl]-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1184)

To a solution of 160 mg of (R)-2-phenyl-2-(trifluoromethoxy)acetic acid (containing impurities) synthesized in the similar manner as in Reference Example 89 in 2 ml of dehydrated dichloromethane, 0.083 ml (0.95 mmol) of oxalyl chloride and 0.006 ml (0.08 mmol) of DMF were added with stirring at 0° C. in an argon atmosphere and stirred at room temperature for 1.5 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 150 mg (0.396 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.350 ml (2.00 mmol) of DIPEA in 2 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 3 ml of dehydrated dichloromethane was added dropwise with stirring at 0° C. in an argon atmosphere and stirred at room temperature for 2 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with water, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 70:30 (V/V)), subsequently concentrated under reduced pressure, and dried under reduced pressure to obtain a concentration residue.

To a solution of the obtained concentration residue in 2 ml of dehydrated dichloromethane, 0.130 ml (1.19 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature in an argon atmosphere and then stirred at room temperature for 2 hours.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate and then added to n-hexane, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 97.6 mg of the title compound (yield: 48%) as a white solid.

Mass spectrum (CI, m/z): 509 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.39-11.84 (m, 1H), 9.58 (br s, 1H), 7.54-7.41 (m, 5H), 6.06 (s, 1H), 4.78 (br d, J=11.9 Hz, 1H), 4.08 (br d, J=11.9 Hz, 1H), 2.58-2.35 (m, 2H), 2.23-2.10 (m, 2H), 1.88-1.73 (m, 2H), 1.70 (s, 3H), 1.60 (s, 3H), 0.04 (s, 9H).

Example 100 (R)—N-[6,6-Dimethyl-5-(2-phenyl-2-propoxyacetyl)-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1196)

To a solution of 146 mg (0.753 mmol) of (R)-2-phenyl-2-propoxyacetic acid synthesized in the similar manner as in Reference Example 91 in 2 ml of dehydrated dichloromethane, 0.10 ml (1.2 mmol) of oxalyl chloride and 0.0050 ml (0.065 mmol) of dehydrated DMF were added in this order at 0° C. in an argon atmosphere and then stirred for 1.5 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure and dried under reduced pressure to obtain a concentration residue.

To a solution of 144 mg (0.380 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.33 ml (1.9 mmol) of DIPEA in 1 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added at 0° C. in an argon atmosphere and then stirred for 1.5 hours with the temperature unchanged.

After the completion of the reaction, ethyl acetate and a saturated aqueous solution of sodium bicarbonate were added to the reaction solution and stirred. After separation into an aqueous layer and an organic layer, the aqueous layer was subjected to extraction with ethyl acetate twice. All of the organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=85:15 to 60:40 (V/V)), subsequently concentrated under reduced pressure, and dried under reduced pressure to obtain a concentration residue.

To a solution of the obtained concentration residue in 2 ml of THF, 0.17 ml (1.6 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature in an argon atmosphere and then stirred at room temperature for 3 hours.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with ethyl acetate three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=85:15 to 60:40 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 144 mg of the title compound (yield: 80%) as a white solid.

Mass spectrum (CI, m/z): 483 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.43-11.75 (m, 1H), 9.56 (br s, 1H), 7.43-7.27 (m, 5H), 5.03 (s, 1H), 4.71-4.47 (m, 1H), 4.39 (br d, J=12.5 Hz, 1H), 3.51-3.43 (m, 1H), 3.41-3.24 (m, 1H), 2.60-2.36 (m, 2H), 2.25-2.10 (m, 2H), 1.88-1.72 (m, 2H), 1.68 (s, 3H), 1.65-1.48 (m, 5H), 0.87 (t, J=7.4 Hz, 3H), 0.04 (s, 9H).

Example 101 N-{5-[2-(4-Fluorophenyl)-2-methoxyacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1427)

To a suspension of 229 mg of 2-(4-fluorophenyl)-2-methoxyacetic acid (containing impurities) synthesized in the similar manner as in Reference Example 93 in 2 ml of dehydrated dichloromethane, 0.150 ml (1.71 mmol) of oxalyl chloride and 0.011 ml (0.14 mmol) of DMF were added with stirring at 0° C. in an argon atmosphere and stirred at room temperature for 1.5 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 265 mg (0.700 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.620 ml (3.55 mmol) of DIPEA in 2 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 3 ml of dehydrated dichloromethane was added dropwise with stirring at 0° C. in an argon atmosphere and stirred at room temperature for 1 hour.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with water, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 70:30 (V/V)), subsequently concentrated under reduced pressure, and dried under reduced pressure to obtain a concentration residue.

To a solution of the obtained concentration residue in 2 ml of dehydrated dichloromethane, 0.230 ml (2.11 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature in an argon atmosphere and then stirred at room temperature for 1 hour.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in dichloromethane, and then, a 5% aqueous potassium bisulfate solution was added thereto, stirred, and separated into an aqueous layer and an organic layer. The obtained organic layer was washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate and then added to n-hexane, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 174 mg of the title compound (yield: 53%) as a white solid.

Mass spectrum (CI, m/z): 473 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.27 & 11.91 (br s, total 1H), 9.58 (br s, 1H), 7.47-7.36 (m, 2H), 7.26-7.14 (m, 2H), 4.99 (s, 1H), 4.76-4.53 (m, 1H), 4.32 (br d, J=12.4 Hz, 1H), 3.29 (s, 3H), 2.58-2.36 (m, 2H), 2.25-2.10 (m, 2H), 1.88-1.72 (m, 2H), 1.69 (br s, 3H), 1.60 (s, 3H), 0.05 (s, 9H).

Example 102 N-{5-[2-(3-Fluorophenyl)-2-methoxyacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1404)

To a suspension of 146 mg of 2-(3-fluorophenyl)-2-methoxyacetic acid (containing impurities) synthesized in the similar manner as in Reference Example 96 in 2 ml of dehydrated dichloromethane, 0.080 ml (0.91 mmol) of oxalyl chloride and 0.010 ml (0.13 mmol) of DMF were added with stirring at 0° C. in an argon atmosphere and stirred at room temperature for 1.5 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 200 mg (0.528 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.462 ml (2.65 mmol) of DIPEA in 2 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 3 ml of dehydrated dichloromethane was added dropwise with stirring at room temperature in an argon atmosphere and stirred at room temperature for 1 hour.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with water, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 70:30 (V/V)), subsequently concentrated under reduced pressure, and dried under reduced pressure to obtain a concentration residue.

To a solution of the obtained concentration residue in 2 ml of dehydrated dichloromethane, 0.173 ml (1.59 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature in an argon atmosphere and then stirred at room temperature for 16 hours.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 187 mg of the title compound (yield: 75%) as a white solid.

Mass spectrum (CI, m/z): 473 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.40-11.81 (m, 1H), 9.60 (br s, 1H), 7.48-7.38 (m, 1H), 7.24-7.13 (m, 3H), 5.03 (s, 1H), 4.75-4.54 (m, 1H), 4.39 (br d, J=12.7 Hz, 1H), 3.32 (s, 3H), 2.59-2.36 (m, 2H), 2.24-2.10 (m, 2H), 1.88-1.72 (m, 2H), 1.69 (s, 3H), 1.60 (s, 3H), 0.05 (s, 9H).

Example 103 (R)—N-{5-[2-(2-Fluorophenyl)-2-methoxyacetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1383)

To a suspension of 200 mg (1.09 mmol) of (R)-2-(2-fluorophenyl)-2-methoxyacetic acid synthesized in the similar manner as in Reference Example 98 in 2 ml of dehydrated dichloromethane, 0.111 ml (1.27 mmol) of oxalyl chloride and 0.010 ml (0.13 mmol) of DMF were added with stirring at 0° C. in an argon atmosphere and stirred at room temperature for 1.5 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 200 mg (0.528 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.500 ml (2.86 mmol) of DIPEA in 2 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 3 ml of dehydrated dichloromethane was added dropwise with stirring at room temperature in an argon atmosphere and stirred at room temperature for 2 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with water, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 70:30 (V/V)), subsequently concentrated under reduced pressure, and dried under reduced pressure to obtain a concentration residue.

To a solution of the obtained concentration residue in 2 ml of dehydrated dichloromethane, 0.173 ml (1.59 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature in an argon atmosphere and then stirred at room temperature for 3 hours.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 164 mg of the title compound (yield: 66%) as a white solid.

Mass spectrum (CI, m/z): 473 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.42-11.83 (m, 1H), 9.60 (br s, 1H), 7.46-7.34 (m, 2H), 7.27-7.18 (m, 2H), 5.22 (s, 1H), 4.75 (d, J=12.3 Hz, 1H), 4.20 (d, J=12.3 Hz, 1H), 3.32 (s, 3H), 2.58-2.37 (m, 2H), 2.25-2.11 (m, 2H), 1.88-1.73 (m, 2H), 1.70 (s, 3H), 1.60 (s, 3H), 0.05 (s, 9H).

Example 104 N-{5-[2-Methoxy-2-(thiophen-2-yl)acetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1546)

To a suspension of 60 mg of 2-methoxy-2-(thiophen-2-yl)acetic acid (containing impurities) synthesized in the similar manner as in Reference Example 101 in 2 ml of dehydrated dichloromethane, 0.036 ml (0.41 mmol) of oxalyl chloride and 0.005 ml (0.07 mmol) of DMF were added with stirring at 0° C. in an argon atmosphere and stirred at room temperature for 1.5 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 120 mg (0.317 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.166 ml (0.950 mmol) of DIPEA in 2 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 3 ml of dehydrated dichloromethane was added dropwise with stirring at 0° C. in an argon atmosphere and stirred at room temperature for 2 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with water, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 70:30 (V/V)), subsequently concentrated under reduced pressure, and dried under reduced pressure to obtain a concentration residue.

To a solution of the obtained concentration residue in 2 ml of dehydrated dichloromethane, 0.104 ml (0.954 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature in an argon atmosphere and then stirred at room temperature for 16 hours.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in methanol and then added to water, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 62 mg of the title compound (yield: 42%) as a white solid.

Mass spectrum (CI, m/z): 461 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.41-11.86 (m, 1H), 9.82-9.47 (m, 1H), 7.57 (dd, J=1.3, 5.0 Hz, 1H), 7.13-7.06 (m, 1H), 7.01 (dd, J=3.5, 5.0 Hz, 1H), 5.26 (s, 1H), 4.84-4.64 (m, 1H), 4.41 (br d, J=12.4 Hz, 1H), 3.28 (s, 3H), 2.58-2.37 (m, 2H), 2.26-2.10 (m, 2H), 1.89-1.73 (m, 2H), 1.70 (s, 3H), 1.62 (s, 3H), 0.06 (s, 9H).

Example 105 (−)-N-{5-[2-Methoxy-2-(thiophen-2-yl)acetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1548)

0.041 g (0.089 mmol) of N-{5-[2-methoxy-2-(thiophen-2-yl)acetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide synthesized in the similar manner as in Example 104 was subjected to optical resolution preparative chromatography (column: CHIRALPAK (trade name) ID, elution solvent: n-hexane:ethanol=85:15 (V/V)), and a fraction containing an optically active form eluted first was concentrated under reduced pressure to obtain 17 mg of the title compound (yield: 41%) as a white solid.

Specific optical rotation: [α]_(D) ²⁰=−51 (c=0.20, methanol).

Mass spectrum (CI, m/z): 461 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.23 (br s, 1H), 9.67 (br s, 1H), 7.57 (dd, J=1.2, 5.0 Hz, 1H), 7.13-7.06 (m, 1H), 7.01 (dd, J=3.5, 5.0 Hz, 1H), 5.26 (s, 1H), 4.74 (br d, J=12.5 Hz, 1H), 4.41 (d, J=12.5 Hz, 1H), 3.28 (s, 3H), 2.58-2.37 (m, 2H), 2.24-2.11 (m, 2H), 1.89-1.74 (m, 2H), 1.70 (s, 3H), 1.62 (s, 3H), 0.06 (s, 9H).

HPLC analysis:

Column: CHIRALPAK (trade name) ID 4.6×250 mm

Eluent: n-hexane/ethanol=85/15 (V/V)

Flow rate: 1.0 ml/min

Temperature: 40° C.

Detection wavelength: 254 nm

Retention time: 7.6 min.

Optical purity: >99% ee

Example 106 (+)-N-{5-[2-Methoxy-2-(thiophen-2-yl)acetyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1547)

A fraction containing an optically active form eluted later in the optical resolution preparative chromatography operation of Example 105 was concentrated under reduced pressure to obtain 14 mg of the title compound (yield: 34%) as a white solid.

Specific optical rotation: [α]_(D) ²⁰=+66° (c=0.20, methanol).

Mass spectrum (CI, m/z): 461 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.23 (br s, 1H), 9.66 (br s, 1H), 7.57 (dd, J=1.2, 5.0 Hz, 1H), 7.14-7.06 (m, 1H), 7.01 (dd, J=3.5, 5.0 Hz, 1H), 5.26 (s, 1H), 4.74 (br d, J=12.4 Hz, 1H), 4.41 (d, J=12.4 Hz, 1H), 3.28 (s, 3H), 2.58-2.37 (m, 2H), 2.26-2.10 (m, 2H), 1.89-1.74 (m, 2H), 1.70 (s, 3H), 1.62 (s, 3H), 0.06 (s, 9H).

HPLC analysis:

Column: CHIRALPAK (trade name) ID 4.6×250 mm

Eluent: n-hexane/ethanol=85/15 (V/V)

Flow rate: 1.0 ml/min

Temperature: 40° C.

Detection wavelength: 254 nm

Retention time: 9.7 min.

Optical purity: >99% ee

Example 107 N-{[1-(Hydroxymethyl)cyclobutyl](phenyl)methyl}-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-718)

To a solution of a mixture of 131 mg (0.243 mmol) of 2-ethyl 5-(trichloromethyl) 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]pyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate synthesized in the similar manner as in Reference Example 102 and 79 mg (0.18 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate in 3 ml of dehydrated 1,4-dioxane, 0.34 ml (2.0 mmol) of DIPEA and 235 mg (1.23 mmol) of {1-[amino(phenyl)methyl]cyclobutyl}methanol synthesized in the similar manner as in Reference Example 103 were added in this order at room temperature in an argon atmosphere and then stirred at 90° C. for 1.5 hours. After standing to cool until the reaction solution becomes room temperature, 0.21 ml (1.9 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature and stirred for 2 hours with the temperature unchanged.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with ethyl acetate three times. All of the organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 187 mg of a white solid. The obtained solid was subjected to preparative HPLC (column: X-Bridge (trade name) ODS, elution solvent: acetonitrile:1 mM aqueous potassium dihydrogen phosphate solution=50:50 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, and acetonitrile was distilled off. The solid deposited in the course of concentration was collected by filtration, washed with water, and then dried under reduced pressure to obtain 156 mg of the title compound (yield: 70%) as a white solid.

Mass spectrum (CI, m/z): 524 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.34-11.78 (m, 1H), 9.87-9.34 (m, 1H), 7.35-7.27 (m, 4H), 7.24-7.16 (m, 1H), 6.75 (d, J=7.9 Hz, 1H), 5.49 (br s, 1H), 4.95 (d, J=7.9 Hz, 1H), 4.47-4.20 (m, 2H), 3.49-3.41 (m, 1H), 3.26-3.18 (m, 1H), 2.57-2.39 (m, 2H), 2.26-2.14 (m, 2H), 2.11-1.99 (m, 2H), 1.98-1.74 (m, 5H), 1.61 (s, 3H), 1.53 (s, 3H), 1.26-1.13 (m, 1H), 0.08 (s, 9H).

Example 108 (R)—N-[2-(1-Hydroxycyclopropyl)-1-phenylethyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-743)

To a solution of 128 mg of (R)-1-(2-amino-2-phenylethyl)cyclopropanol (containing impurities) synthesized in the similar manner as in Reference Example 105 in 2 ml of dehydrated 1,4-dioxane, 0.26 ml (1.5 mmol) of DIPEA and 154 mg (0.349 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 were added in this order at room temperature in an argon atmosphere and then stirred at 90° C. for 2 hours. After standing to cool until the reaction solution becomes room temperature, 0.16 ml (1.5 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature and stirred for 2 hours with the temperature unchanged.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with ethyl acetate twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=70:30 to 40:60 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was suspended in an ethyl acetate/n-hexane mixed solvent and stirred, and then, insoluble matter was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 139 mg of the title compound (yield: 79%) as a white solid.

Mass spectrum (CI, m/z): 510 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.23 & 11.80 (br s, total 1H), 9.75-9.47 (m, 1H), 7.43-7.37 (m, 2H), 7.34-7.27 (m, 2H), 7.23-7.17 (m, 1H), 6.51-6.33 (m, 1H), 5.54-5.37 (m, 1H), 5.14-5.05 (m, 1H), 4.66-4.29 (m, 2H), 2.61-2.39 (m, 2H), 2.26-2.06 (m, 3H), 1.90-1.50 (m, 9H), 0.55-0.37 (m, 3H), 0.18-0.04 (m, 10H).

Example 109 (R)—N-(3-Ethyl-3-Hydroxy-1-phenylpentyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-759)

To a solution of 118 mg (0.568 mmol) of (R)-1-amino-3-ethyl-1-phenylpentan-3-ol synthesized in the similar manner as in Reference Example 107 in 2 ml of dehydrated 1,4-dioxane, 0.20 ml (1.1 mmol) of DIPEA and 128 mg (0.290 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 were added in this order at room temperature in an argon atmosphere and then stirred at 90° C. for 2 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred, followed by extraction with ethyl acetate three times. All of the organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=75:25 to 40:60 (V/V)), subsequently concentrated under reduced pressure, and dried under reduced pressure to obtain a concentration residue.

To a solution of the obtained concentration residue in 2 ml of THF, 0.13 ml (1.2 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature in an argon atmosphere and then stirred at room temperature for 2 hours.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with ethyl acetate three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=70:30 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was suspended in an ethyl acetate/n-hexane mixed solvent and stirred at room temperature, and then, insoluble matter was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 123 mg of the title compound (yield: 79%) as a white solid.

Mass spectrum (CI, m/z): 540 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.35-11.68 (m, 1H), 9.56 (br s, 1H), 7.37-7.24 (m, 4H), 7.19-7.13 (m, 1H), 6.56 (d, J=5.8 Hz, 1H), 4.91-4.81 (m, 1H), 4.54-4.31 (m, 3H), 2.58-2.41 (m, 2H), 2.26-2.13 (m, 2H), 1.95-1.73 (m, 3H), 1.63-1.55 (m, 4H), 1.53 (s, 3H), 1.49-1.33 (m, 4H), 0.82 (t, J=7.4 Hz, 3H), 0.77 (t, J=7.4 Hz, 3H), 0.09 (s, 9H).

Example 110 (R)—N-[1-(4-Fluorophenyl)-3-hydroxy-3-methylbutyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-939)

To a solution of 599 mg (1.36 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 3 ml of 1,4-dioxane, 134 mg of (R)-4-amino-4-(4-fluorophenyl)-2-methylbutan-2-ol (containing impurities) synthesized in the similar manner as in Reference Example 111 and 0.602 ml (3.40 mmol) of DIPEA were added in this order at room temperature under argon stream and then stirred at 100° C. for 1 hour. Subsequently, 0.318 ml (3.40 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature and stirred for 2 hours with the temperature unchanged.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride in this order, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: ethyl acetate:methanol=100:0 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected to preparative HPLC (column: X-Bridge (trade name) ODS, elution solvent: acetonitrile:1 mM aqueous potassium dihydrogen phosphate solution=30:70 to 50:50 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, and acetonitrile was distilled off, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, then filtered, concentrated under reduced pressure, and dried under reduced pressure to obtain 48 mg of the title compound (yield: 8% [2 steps]) as a white solid.

Mass spectrum (CI, m/z): 530 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.77 (br s, total 1H), 9.74-9.41 (m, 1H), 7.40-7.32 (m, 2H), 7.14-7.05 (m, 2H), 6.66-6.44 (m, 1H), 4.94-4.84 (m, 1H), 4.75-4.60 (m, 1H), 4.52-4.31 (m, 2H), 2.59-2.39 (m, 2H), 2.27-2.11 (m, 2H), 2.04-1.73 (m, 3H), 1.70-1.45 (m, 7H), 1.15 (s, 3H), 1.13 (s, 3H), 0.09 (s, 9H).

Example 111 (R)—N-[1-(3-Fluorophenyl)-3-hydroxy-3-methylbutyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-911)

To a solution of 149 mg (0.248 mmol) of (R)-ethyl 5-{[1-(3-fluorophenyl)-3-hydroxy-3-methylbutyl]carbamoyl}-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 116 in 3 ml of dichloromethane, 0.108 ml (0.992 mmol) of N,N-dimethylethane-1,2-diamine was added in one portion with stirring at room temperature under argon stream and stirred at room temperature for 1 hour.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate twice. The organic layer was washed with a 5% aqueous potassium bisulfate solution, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=70:30 to 17:83 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in a small amount of ethyl acetate, and a solid was deposited by adding n-hexane. The solid was collected by filtration, washed with n-hexane, and dried under reduced pressure at 50° C. to obtain 101 mg of the title compound (yield: 77%) as a white solid.

Mass spectrum (CI, m/z): 530 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.77 (br s, total 1H), 9.71-9.47 (m, 1H), 7.37-7.26 (m, 1H), 7.22-7.11 (m, 2H), 7.02-6.92 (m, 1H), 6.65-6.51 (m, 1H), 4.95-4.87 (m, 1H), 4.76-4.60 (m, 1H), 4.55-4.35 (m, 2H), 2.57-2.40 (m, 2H), 2.27-2.12 (m, 2H), 2.03-1.74 (m, 3H), 1.66 (dd, J=3.1, 14.2 Hz, 1H), 1.59 (br s, 3H), 1.54 (br s, 3H), 1.16 (s, 3H), 1.13 (s, 3H), 0.09 (s, 9H).

Example 112 (R)—N-[1-(2-Fluorophenyl)-3-hydroxy-3-methylbutyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-883)

To a solution of 150 mg (0.249 mmol) of (R)-ethyl 5-{[1-(2-fluorophenyl)-3-hydroxy-3-methylbutyl]carbamoyl}-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 121 in 3 ml of dichloromethane, 0.109 ml (1.00 mmol) of N,N-dimethylethane-1,2-diamine was added in one portion with stirring at room temperature under argon stream and stirred at room temperature for 1 hour.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate twice. The organic layer was washed with a 5% aqueous potassium bisulfate solution, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=70:30 to 17:83 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in a small amount of ethyl acetate, and a solid was deposited by adding n-hexane. The solid was collected by filtration, washed with n-hexane, and dried under reduced pressure at 50° C. to obtain 112 mg of the title compound (yield: 85%) as a white solid.

Mass spectrum (CI, m/z): 530 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.20 & 11.76 (br s, total 1H), 9.72-9.46 (m, 1H), 7.54-7.43 (m, 1H), 7.26-7.17 (m, 1H), 7.17-7.04 (m, 2H), 6.62-6.47 (m, 1H), 5.23-5.14 (m, 1H), 4.78-4.62 (m, 1H), 4.55-4.35 (m, 2H), 2.58-2.40 (m, 2H), 2.27-2.12 (m, 2H), 2.02-1.73 (m, 3H), 1.67-1.45 (m, 7H), 1.18 (s, 3H), 1.15 (s, 3H), 0.09 (s, 9H).

Example 113 (R)—N-(5-Hydroxy-2,5-dimethylhexan-3-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-815)

To a solution of 99 mg (0.18 mmol) of (R)-ethyl 5-[(5-hydroxy-2,5-dimethylhexan-3-yl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 125 in 3 ml of dichloromethane, 0.078 ml (0.72 mmol) of N,N-dimethylethane-1,2-diamine was added in one portion with stirring at room temperature under argon stream and stirred at room temperature for 1 hour.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate twice. The organic layer was washed with a 5% aqueous potassium bisulfate solution, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=50:50 to 16:84 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in a small amount of ethyl acetate, and a solid was deposited by adding n-hexane. The solid was collected by filtration, washed with n-hexane, and dried under reduced pressure at 50° C. to obtain 72 mg of the title compound (yield: 84%) as a white solid.

Mass spectrum (CI, m/z): 478 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.19 & 11.81 (br s, total 1H), 9.71-9.44 (m, 1H), 5.63 (br s, 1H), 4.47-4.25 (m, 3H), 3.71-3.60 (m, 1H), 2.57-2.39 (m, 2H), 2.27-2.11 (m, 2H), 1.90-1.66 (m, 3H), 1.65-1.52 (m, 7H), 1.49-1.42 (m, 1H), 1.10 (s, 3H), 1.09 (s, 3H), 0.82 (d, J=6.8 Hz, 6H), 0.08 (s, 9H).

Example 114 N-[1-(4-Fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-946)

To a solution of 0.745 g (1.69 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 8 ml of 1,4-dioxane, 1.47 ml (8.44 mmol) of DIPEA and 1.00 g (5.07 mmol) of 3-amino-3-(4-fluorophenyl)-2,2-dimethylpropan-1-ol synthesized in the similar manner as in Reference Example 127 were added in this order with stirring at room temperature under argon stream and stirred at 90° C. for 1.5 hours. Subsequently, the reaction solution was allowed to cool to room temperature, and then, 0.738 ml (6.78 mmol) of N,N-dimethylethane-1,2-diamine was added dropwise at room temperature and stirred at room temperature for 4 hours.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate twice. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=70:30 to 19:81 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The concentration residue was dissolved in 60 ml of ethyl acetate and washed with 10 ml of a 5% aqueous potassium bisulfate solution three times. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was dissolved in a small amount of ethyl acetate, and a solid was deposited by adding n-hexane. The solid was collected by filtration, washed with n-hexane, and dried under reduced pressure at 50° C. to obtain 509 mg of the title compound (yield: 57%) as a white solid.

Mass spectrum (ESI, m/z): 530 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.80 (br s, total 1H), 9.68-9.44 (m, 1H), 7.39-7.32 (m, 2H), 7.17-7.09 (m, 2H), 6.91-6.78 (m, 1H), 5.46 (br s, 1H), 4.65 (d, J=7.9 Hz, 1H), 4.45-4.28 (m, 2H), 3.23 (dd, J=4.2, 10.6 Hz, 1H), 3.08-2.99 (m, 1H), 2.60-2.39 (m, 2H), 2.27-2.14 (m, 2H), 1.91-1.73 (m, 2H), 1.65-1.49 (m, 6H), 1.05 (s, 3H), 0.64 (s, 3H), 0.09 (s, 9H).

Example 115 N-[1-(3-Fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-918)

To a solution of 162 mg (0.367 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 4 ml of 1,4-dioxane, 0.32 ml (1.9 mmol) of DIPEA and 227 mg (1.15 mmol) of 3-amino-3-(3-fluorophenyl)-2,2-dimethylpropan-1-ol synthesized in the similar manner as in Reference Example 129 were added at room temperature in an argon atmosphere and then reacted at 100° C. for 2.5 hours. After standing to cool, 0.12 ml (1.1 mmol) of N,N-dimethyl-1,2-diamine was added and stirred at room temperature for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, 20 ml of ethyl acetate was added to the residue, the organic layer after washing with 10 ml of a 5% aqueous potassium bisulfate solution, 10 ml of a saturated aqueous solution of sodium bicarbonate, and 10 ml of a saturated aqueous solution of sodium chloride in this order was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=81:19 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in a small amount of dichloromethane, then n-hexane was added, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 159 mg of the title compound (yield: 82%) as a white solid.

Mass spectrum (CI, m/z): 530 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.22 & 11.89 (br s, total 1H), 9.79-9.40 (m, 1H), 7.39-7.29 (m, 1H), 7.22-7.13 (m, 2H), 7.08-7.01 (m, 1H), 6.86 (d, J=8.0 Hz, 1H), 5.56-5.41 (m, 1H), 4.67 (d, J=8.0 Hz, 1H), 4.49-4.27 (m, 2H), 3.25 (dd, J=4.0, 10.6 Hz, 1H), 3.05 (dd, J=4.0, 10.6 Hz, 1H), 2.56-2.40 (m, 2H), 2.29-2.13 (m, 2H), 1.92-1.72 (m, 2H), 1.60 (br s, 3H), 1.52 (br s, 3H), 1.05 (s, 3H), 0.67 (s, 3H), 0.09 (s, 9H).

Example 116 (−)-N-[1-(3-Fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-920)

0.129 g (0.244 mmol) of N-[1-(3-fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide synthesized in the similar manner as in Example 115 was subjected to optical resolution preparative chromatography (column: CHIRALPAK (trade name) ID, elution solvent: n-hexane:ethanol:methanol=95:5:1 (V/V)), and a fraction containing an optically active form eluted first was concentrated under reduced pressure to obtain 47 mg of the title compound (yield: 36%) as a white solid.

Specific optical rotation: [α]_(D) ²⁰=−53° (c=0.23, methanol).

Mass spectrum (CI, m/z): 530 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.88 (br s, total 1H), 9.78-9.41 (m, 1H), 7.38-7.30 (m, 1H), 7.21-7.13 (m, 2H), 7.08-7.01 (m, 1H), 6.86 (br d, J=8.3 Hz, 1H), 5.56-5.40 (m, 1H), 4.67 (d, J=8.3 Hz, 1H), 4.47-4.30 (m, 2H), 3.25 (br dd, J=3.9, 10.5 Hz, 1H), 3.05 (br dd, J=3.9, 10.5 Hz, 1H), 2.60-2.40 (m, 2H), 2.26-2.13 (m, 2H), 1.90-1.73 (m, 2H), 1.60 (br s, 3H), 1.52 (s, 3H), 1.05 (s, 3H), 0.67 (s, 3H), 0.09 (s, 9H).

HPLC analysis:

Column: CHIRALPAK (trade name) ID 4.6×250 mm

Eluent: n-hexane/ethanol/methanol=95/5/1 (V/V)

Flow rate: 1.0 ml/min

Temperature: 40° C.

Detection wavelength: 254 nm

Retention time: 8.8 min.

Optical purity: >99% ee

Example 117 (+)-N-[1-(3-Fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-919)

A fraction containing an optically active form eluted later in the optical resolution preparative chromatography operation of Example 116 was concentrated under reduced pressure to obtain 45 mg of the title compound (yield: 35%) as a white solid.

Specific optical rotation: [α]_(D) ²⁰=+59° (c=0.22, methanol).

Mass spectrum (CI, m/z): 530 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.94 (br s, total 1H), 9.78-9.41 (m, 1H), 7.38-7.30 (m, 1H), 7.21-7.13 (m, 2H), 7.08-7.01 (m, 1H), 6.86 (br d, J=8.1 Hz, 1H), 5.56-5.39 (m, 1H), 4.67 (d, J=8.1 Hz, 1H), 4.47-4.30 (m, 2H), 3.25 (br dd, J=3.8, 10.5 Hz, 1H), 3.05 (br dd, J=3.8, 10.5 Hz, 1H), 2.59-2.40 (m, 2H), 2.27-2.13 (m, 2H), 1.90-1.73 (m, 2H), 1.60 (br s, 3H), 1.52 (s, 3H), 1.05 (s, 3H), 0.67 (s, 3H), 0.09 (s, 9H).

HPLC analysis:

Column: CHIRALPAK (trade name) ID 4.6×250 mm

Elution solvent: n-hexane/ethanol/methanol=95/5/1 (V/V)

Flow rate: 1.0 ml/min

Temperature: 40° C.

Detection wavelength: 254 nm

Retention time: 11.6 min.

Optical purity: >98% ee

Example 118 N-[1-(2-Fluorophenyl)-3-hydroxy-2,2-dimethylpropyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-890)

To a solution of 225 mg (1.14 mmol) of 3-amino-3-(2-fluorophenyl)-2,2-dimethylpropan-1-ol synthesized in the similar manner as in Reference Example 130 in 4 ml of 1,4-dioxane, 0.32 ml (1.9 mmol) of DIPEA and 166 mg (0.376 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarbox amido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 were added at room temperature in an argon atmosphere and then reacted at 100° C. for 2.5 hours. After standing to cool, 0.12 ml (1.1 mmol) of N,N-dimethylethane-1,2-diamine was added and stirred at room temperature for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, 20 ml of ethyl acetate was added to the residue, the organic layer after washing with 10 ml of a 5% aqueous potassium bisulfate solution, 10 ml of a saturated aqueous solution of sodium bicarbonate, and 10 ml of a saturated aqueous solution of sodium chloride in this order was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=81:19 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in a small amount of dichloromethane, then n-hexane was added, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 154 mg of the title compound (yield: 77%) as a white solid.

Mass spectrum (CI, m/z): 530 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.22 & 11.87 (br s, total 1H), 9.75-9.42 (m, 1H), 7.53-7.44 (m, 1H), 7.32-7.24 (m, 1H), 7.23-7.17 (m, 1H), 7.17-7.08 (m, 1H), 6.96-6.85 (m, 1H), 5.53 (br s, 1H), 5.03 (d, J=7.9 Hz, 1H), 4.46-4.26 (m, 2H), 3.40-3.28 (m, 1H), 3.08 (dd, J=4.0, 10.5 Hz, 1H), 2.56-2.39 (m, 2H), 2.27-2.12 (m, 2H), 1.92-1.72 (m, 2H), 1.65-1.47 (m, 6H), 1.10 (s, 3H), 0.69-0.60 (m, 3H), 0.09 (s, 9H).

Example 119 N-(1-Hydroxy-2,2,4-trimethylpentan-3-yl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-822)

To a solution of a mixture of 133 mg (0.246 mmol) of 2-ethyl 5-(trichloromethyl) 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]pyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate synthesized in the similar manner as in Reference Example 102 and 80 mg (0.18 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate in 3 ml of dehydrated 1,4-dioxane, 0.37 ml (2.1 mmol) of DIPEA and 189 mg (1.30 mmol) of 3-amino-2,2,4-trimethylpentan-1-ol synthesized in the similar manner as in Reference Example 132 were added in this order at room temperature in an argon atmosphere and then stirred at 90° C. for 2.5 hours. After standing to cool until the reaction solution becomes room temperature, 0.23 ml (2.1 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature and stirred for 14 hours with the temperature unchanged.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with ethyl acetate three times. All of the organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 107 mg of the title compound (yield: 52%) as a white solid.

Mass spectrum (CI, m/z): 478 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.42-11.70 (m, 1H), 9.86-9.33 (m, 1H), 5.48 (br d, J=9.2 Hz, 1H), 5.13-4.93 (m, 1H), 4.48-4.22 (m, 2H), 3.55-3.48 (m, 1H), 3.45 (dd, J=3.9, 10.7 Hz, 1H), 3.04 (dd, J=5.4, 10.7 Hz, 1H), 2.58-2.38 (m, 2H), 2.26-2.12 (m, 2H), 2.05-1.92 (m, 1H), 1.88-1.73 (m, 2H), 1.61 (br s, 3H), 1.59 (br s, 3H), 0.93 (s, 3H), 0.89 (d, J=6.7 Hz, 6H), 0.79 (s, 3H), 0.07 (s, 9H).

Example 120 (R)—N-(3-Hydroxy-3-methyl-1-phenylbutyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. III-298)

To a solution of 1.53 g (4.19 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 46 in 20 ml of dehydrated dichloromethane, 2.60 ml (14.9 mmol) of DIPEA was added at room temperature in an argon atmosphere. Subsequently, a solution of 700 mg (2.36 mmol) of bis(trichloromethyl) carbonate in 5 ml of dehydrated dichloromethane was added dropwise at −78° C. and then stirred for 0.5 hours with the temperature unchanged and further for 2 hours after the temperature was raised to room temperature.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate and dichloromethane were added to the reaction solution at −78° C. and then stirred for 1.5 hours while the temperature was raised to room temperature for a while. The reaction solution was separated into an aqueous layer and an organic layer, and then, the aqueous layer was subjected to extraction with ethyl acetate twice. All of the organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=85:15 to 75:25 (V/V)), subsequently concentrated under reduced pressure, and dried under reduced pressure to obtain 1.75 g of a white solid.

To a solution of 97.1 mg (0.542 mmol) of (R)-4-amino-2-methyl-4-phenylbutan-2-ol synthesized in the similar manner as in Reference Example 23 in 2 ml of dehydrated 1,4-dioxane, 0.18 ml (1.0 mmol) of DIPEA and 130 mg of a portion of the solid obtained by the operation described above were added in this order at room temperature in an argon atmosphere and then stirred at 90° C. for 1.5 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred, followed by extraction with ethyl acetate three times. All of the organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=70:30 to 30:70 (V/V)), subsequently concentrated under reduced pressure, and dried under reduced pressure to obtain a concentration residue.

To a solution of the obtained concentration residue in 2 ml of THF, 0.12 ml (1.1 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature in an argon atmosphere and then stirred for 2 hours with the temperature unchanged.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with ethyl acetate three times. All of the organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=50:50 to 25:75 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 96 mg of the title compound (yield: 62% [2 steps]) as a white solid.

Mass spectrum (CI, m/z): 498 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.35-11.77 (m, 1H), 9.95-9.67 (m, 1H), 7.36-7.23 (m, 4H), 7.19-7.11 (m, 1H), 6.58-6.44 (m, 1H), 4.94-4.84 (m, 1H), 4.64 (br s, 1H), 4.40 (br s, 2H), 2.00-1.88 (m, 1H), 1.65 (dd, J=3.2, 14.2 Hz, 1H), 1.57 (br s, 3H), 1.52 (br s, 3H), 1.16 (s, 3H), 1.13 (s, 3H), 0.97 (br s, 2H), 0.98 (br s, 2H), 0.03 (s, 9H).

Example 121 N-(3-Hydroxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. III-353)

To a solution of 1.53 g (4.19 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 46 in 20 ml of dehydrated dichloromethane, 2.60 ml (14.9 mmol) of DIPEA was added at room temperature in an argon atmosphere. Subsequently, a solution of 700 mg (2.36 mmol) of bis(trichloromethyl) carbonate in 5 ml of dehydrated dichloromethane was added dropwise at −78° C. and then stirred for 0.5 hours with the temperature unchanged and further for 2 hours after the temperature was raised to room temperature.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate and dichloromethane were added to the reaction solution at −78° C. and then stirred for 1.5 hours while the temperature was raised to room temperature for a while. The reaction solution was separated into an aqueous layer and an organic layer, and then, the aqueous layer was subjected to extraction with ethyl acetate twice. All of the organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=85:15 to 75:25 (V/V)), subsequently concentrated under reduced pressure, and dried under reduced pressure to obtain 1.75 g of a white solid.

To a solution of 109 mg (0.608 mmol) of 3-amino-2,2-dimethyl-3-phenylpropan-1-ol [synthesized according to the method described in Synthetic Communications 1994, 24 (7), 899-906] in 2 ml of dehydrated 1,4-dioxane, 0.20 ml (1.1 mmol) of DIPEA and 142 mg of a portion of the solid obtained by the operation described above were added in this order at room temperature in an argon atmosphere and then stirred at 90° C. for 2.5 hours. After standing to cool until the reaction solution becomes room temperature, 0.13 ml (1.2 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature and stirred for 2 hours with the temperature unchanged.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with ethyl acetate three times. All of the organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 40:60 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 112 mg of the title compound (yield: 66% [2 steps]) as a white solid.

Mass spectrum (CI, m/z): 498 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.40-11.84 (m, 1H), 10.11-9.58 (m, 1H), 7.37-7.26 (m, 4H), 7.25-7.18 (m, 1H), 6.85 (br d, J=8.2 Hz, 1H), 5.53-5.39 (m, 1H), 4.63 (d, J=8.2 Hz, 1H), 4.45-4.25 (m, 2H), 3.29-3.22 (m, 1H), 3.07-2.98 (m, 1H), 1.58 (s, 3H), 1.51 (s, 3H), 1.06 (s, 3H), 1.03-0.94 (m, 2H), 0.76-0.58 (m, 5H), 0.03 (s, 9H).

Example 122 (−)-N-(3-Hydroxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-673)

To a solution of a mixture of 545 mg (1.16 mmol) of 2-ethyl 5-(trichloromethyl) 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]pyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate synthesized in the similar manner as in Reference Example 102 and 329 mg (0.853 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate in 7 ml of dehydrated 1,4-dioxane, 1.80 ml (10.3 mmol) of DIPEA and 1.16 g (6.47 mmol) of 3-amino-2,2-dimethyl-3-phenylpropan-1-ol [synthesized according to the method described in Synthetic Communications 1994, 24 (7), 899-906] were added in this order at room temperature in an argon atmosphere and then stirred at 90° C. for 2 hours. After standing to cool until the reaction solution becomes room temperature, 0.90 ml (8.3 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature and stirred for 2.5 hours with the temperature unchanged.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with ethyl acetate three times. All of the organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 40:60 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=100:0 to 85:15 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in an ethyl acetate/ethanol mixed solvent, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 802 mg of a white solid.

0.50 g of a portion of the obtained solid was subjected to optical resolution preparative chromatography (column: CHIRALPAK (trade name) ID, elution solvent: n-hexane:ethanol=90:10 (V/V)), and a fraction containing an optically active form eluted first was concentrated under reduced pressure. The obtained concentration residue was dissolved in an acetonitrile/water mixed solvent and then freeze-dried to obtain 225 mg of the title compound (yield: 35%) as a white solid.

Specific optical rotation: [α]_(D) ²⁰=−66° (c=0.50, methanol).

Mass spectrum (CI, m/z): 512 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.35-11.77 (m, 1H), 9.86-9.35 (m, 1H), 7.36-7.27 (m, 4H), 7.25-7.17 (m, 1H), 6.86 (br d, J=8.2 Hz, 1H), 5.45 (br s, 1H), 4.64 (d, J=8.2 Hz, 1H), 4.46-4.30 (m, 2H), 3.45-3.23 (m, 1H), 3.06-2.99 (m, 1H), 2.58-2.40 (m, 2H), 2.26-2.14 (m, 2H), 1.90-1.73 (m, 2H), 1.60 (s, 3H), 1.52 (s, 3H), 1.06 (s, 3H), 0.64 (s, 3H), 0.09 (s, 9H).

SFC (supercritical fluid chromatography) analysis:

Column: CHIRALPAK (trade name) ID 2.1×150 mm (particle size: 3 um)

Eluent: CO₂/methanol=90/10 (V/V)

Flow rate: 0.85 ml/min

Temperature: 40° C.

Detection wavelength: 240 nm

Retention time: 5.3 min.

Optical purity: >99% ee

Example 123 (+)-N-(3-Hydroxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-672)

A fraction containing an optically active form eluted later in the optical resolution preparative chromatography operation of Example 122 was concentrated under reduced pressure. The obtained concentration residue was dissolved in an acetonitrile/water mixed solvent and then freeze-dried to obtain 223 mg of the title compound (yield: 35%) as a white solid.

Specific optical rotation: [α]_(D) ²⁰=+60° (c=0.50, methanol).

Mass spectrum (CI, m/z): 512 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.42-11.76 (m, 1H), 9.57 (br s, 1H), 7.35-7.27 (m, 4H), 7.25-7.18 (m, 1H), 6.86 (br d, J=8.2 Hz, 1H), 5.45 (br s, 1H), 4.64 (d, J=8.2 Hz, 1H), 4.44-4.30 (m, 2H), 3.44-3.23 (m, 1H), 3.06-2.98 (m, 1H), 2.59-2.40 (m, 2H), 2.26-2.14 (m, 2H), 1.89-1.74 (m, 2H), 1.60 (s, 3H), 1.52 (s, 3H), 1.06 (s, 3H), 0.64 (s, 3H), 0.09 (s, 9H).

SFC (supercritical fluid chromatography) analysis:

Column: CHIRALPAK (trade name) ID 2.1×150 mm (particle size: 3 um)

Eluent: CO₂/methanol=90/10 (V/V)

Flow rate: 0.85 ml/min

Temperature: 40° C.

Detection wavelength: 240 nm

Retention time: 6.5 min.

Optical purity: >99% ee

Example 124 (R)—N-[5-(2-Butoxy-2-phenylacetyl)-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl]-1-(trimethylsilyl)cyclobutanecarboxamide (Compound No. IV-1200)

To a solution of 1.65 g (5.53 mmol) of (R)-benzyl 2-butoxy-2-phenylacetate synthesized in the similar manner as in Reference Example 133 in 8 ml of methanol/8 ml of water, 300 mg (7.15 mmol) of lithium hydroxide monohydrate was added at room temperature and then reacted with stirring at room temperature for 3 hours.

After the completion of the reaction, diethyl ether was added to the reaction solution and separated into an aqueous layer and an organic layer. The aqueous layer was adjusted to pH 2 by adding 2 N hydrochloric acid, followed by extraction with ethyl acetate three times. All of the obtained organic layers were washed with saturated saline, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to obtain 1.34 g of a concentration residue.

To a solution of 150 mg of a portion of the obtained concentration residue in 2 ml of dehydrated dichloromethane, 0.006 ml (0.08 mmol) of DMF and 0.083 ml (0.95 mmol) of oxalyl chloride were added with stirring at 0° C. in an argon atmosphere and stirred at room temperature for 1.5 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 150 mg (0.396 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.350 ml (2.00 mmol) of DIPEA in 2 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 3 ml of dehydrated dichloromethane was added dropwise with stirring at 0° C. in an argon atmosphere and stirred at room temperature for 3 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with water, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 70:30 (V/V)) and subsequently concentrated under reduced pressure to obtain a concentration residue.

To a solution of the obtained concentration residue in 2 ml of dehydrated dichloromethane, 0.130 ml (1.19 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature in an argon atmosphere and then stirred at room temperature for 16 hours.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution and stirred, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium bicarbonate and saturated saline in this order, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected to preparative HPLC (column: X-Bridge (trade name) ODS, elution solvent: acetonitrile:1 mM aqueous potassium dihydrogen phosphate solution=50:50 (V/V)), and ethyl acetate and water were added to a fraction containing the compound of interest to separate an organic layer and an aqueous layer. The obtained organic layer was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate and then added to n-hexane, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 77 mg of the title compound (yield: 39%) as a white solid.

Mass spectrum (CI, m/z): 497 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.34-11.89 (m, 1H), 9.56 (br s, 1H), 7.45-7.25 (m, 5H), 5.02 (s, 1H), 4.68-4.49 (m, 1H), 4.40 (br d, J=12.7 Hz, 1H), 3.57-3.39 (m, 2H), 2.59-2.35 (m, 2H), 2.24-2.09 (m, 2H), 1.87-1.73 (m, 2H), 1.68 (s, 3H), 1.61 (s, 3H), 1.56-1.45 (m, 2H), 1.40-1.28 (m, 2H), 0.86 (t, J=7.3 Hz, 3H), 0.05 (s, 9H).

Example 125 N-(3-Methoxy-2,2-dimethyl-1-phenylpropyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxamide (Compound No. IV-676)

To a solution of 131 mg (0.219 mmol) of ethyl 5-[(3-methoxy-2,2-dimethyl-1-phenylpropyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 137 in 3 ml of dichloromethane, 0.095 ml (0.87 mol) of N,N-dimethylethane-1,2-diamine was added in one portion with stirring at room temperature under argon stream and stirred at room temperature for 1 hour.

After the completion of the reaction, a 5% aqueous potassium bisulfate solution was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate twice. The organic layer was washed with a 5% aqueous potassium bisulfate solution, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=70:30 to 13:87 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was dissolved in a small amount of ethyl acetate, and a solid was deposited by adding n-hexane. The solid was collected by filtration, washed with n-hexane, and dried under reduced pressure at 50° C. to obtain 62 mg of the title compound (yield: 54%) as a white solid.

Mass spectrum (CI, m/z): 526 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.21 & 11.76 (br s, total 1H), 9.58 (br s, 1H), 7.38-7.18 (m, 5H), 6.75-6.52 (m, 1H), 4.59 (d, J=7.7 Hz, 1H), 4.52-4.30 (m, 2H), 3.38 (s, 3H), 3.13 (d, J=9.3 Hz, 1H), 2.92 (d, J=9.3 Hz, 1H), 2.58-2.40 (m, 2H), 2.29-2.12 (m, 2H), 1.91-1.74 (m, 2H), 1.59 (br s, 3H), 1.50 (s, 3H), 1.12 (s, 3H), 0.68 (s, 3H), 0.09 (s, 9H).

Reference Example 1 1-(Trimethylsilyl)cyclobutanecarboxylic acid

To 200 ml of dehydrated THF, 214 ml (428 mmol) of 2 M lithium diisopropylamide/THF solution was added in an argon atmosphere, and then, 10.1 ml (107 mmol) of cyclobutanecarboxylic acid was added dropwise with stirring under cooling in ice water and stirred for 4 hours while the temperature was raised to room temperature for a while. Subsequently, 20 ml (116 mmol) of hexamethylphosphoric acid triamide was added, and 51 ml (490 mmol) of chlorotrimethylsilane was added dropwise with stirring while the internal temperature was kept at −60° C. or lower under cooling in a dry ice/acetone coolant, and then stirred at −78° C. for 16.5 hours.

After the completion of the reaction, 67 ml of methanol was added to the reaction solution, and 134 ml of cold water was added after the temperature was raised to 0° C. The pH was adjusted to 2.1 by adding 2 N hydrochloric acid, 268 ml of diethyl ether was added thereto and then the aqueous layer and the organic layer were separated, and the organic layer was washed with 268 ml of a saturated aqueous solution of sodium chloride. The organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. 50 ml of a 2 N aqueous sodium hydroxide solution and 267 ml of n-hexane were added to the obtained concentration residue and then the aqueous layer and the organic layer were separated. Subsequently, the aqueous layer was adjusted to pH 2.7 by adding 1 N hydrochloric acid, and 267 ml of ethyl acetate was added to this solution and then the aqueous layer and the organic layer were separated. The obtained organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. n-Hexane was added to the obtained concentration residue and cooled in an ice water bath. The resulting solid was filtered, washed by sousing with cooled n-hexane, and then dried under reduced pressure to obtain 6.24 g of the title compound (yield: 34%) as a white solid. The filtrate was further concentrated under reduced pressure, and the obtained residue was subjected to silica gel column chromatography (elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 4.33 g of the title compound (yield: 23%) as a white solid.

Mass spectrum (CI, m/z): 173 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 11.64 (br s, 1H), 2.45-2.34 (m, 2H), 2.17-2.06 (m, 2H), 1.91-1.70 (m, 2H), 0.06 (s, 9H).

Reference Example 2 5-tert-Butyl 2-ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]pyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate

To a solution of 13.9 g (80.4 mmol) of 1-(trimethylsilyl)cyclobutanecarboxylic acid synthesized in the similar manner as in Reference Example 1 in 105 ml of dehydrated dichloromethane, 6.96 ml (81.2 mmol) of oxalyl chloride and 0.32 ml (4.14 mmol) of DMF were added dropwise in this order between −25° C. and −10° C. in an argon atmosphere and then stirred for 2 hours after the temperature was raised to 0° C. To a solution of 8.74 g (26.9 mmol) of 5-tert-butyl 2-ethyl 3-amino-6,6-dimethylpyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate [synthesized according to the method described in Journal of Medicinal Chemistry 2012, 55 (10), 4728-4739] and 23.5 ml (135 mmol) of DIPEA in 122 ml of dehydrated dichloromethane, the resulting reaction solution was added dropwise at 0° C. in an argon atmosphere and stirred at the same temperature as above for 16 hours.

After the completion of the reaction, 486 ml of a 5% aqueous potassium bisulfate solution was added to the reaction solution and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with 200 ml of dichloromethane twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=86:14 to 53:47 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 8.30 g of the title compound (yield: 64%) as a white foam.

Mass spectrum (CI, m/z): 479 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.98 & 9.72 & 9.71 (s, total 1H), 4.50-4.37 (m, 4H), 2.53-2.43 (m, 2H), 2.32-2.07 (m, 2H), 2.02-1.72 (m, 2H), 1.65-1.55 (m, 6H), 1.51-1.42 (m, 9H), 1.38-1.31 (m, 3H), 0.10 & 0.06 & 0.01 (s, total 9H).

Reference Example 3 Ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate

To a solution of 8.30 g (17.3 mmol) of 5-tert-butyl 2-ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]pyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate synthesized in the similar manner as in Reference Example 2 in 81 ml of dehydrated dichloromethane, 6.0 ml (52 mmol) of 2,6-lutidine and 9.2 ml (51 mmol) of trimethylsilyl trifluoromethanesulfonate were added dropwise in this order at 0° C. in an argon atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, 64 ml of a saturated aqueous solution of sodium bicarbonate and 64 ml of dichloromethane were added to the reaction solution and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with 72 ml of dichloromethane twice, and then, all of the obtained organic layers were washed with 72 ml of a saturated aqueous solution of sodium bicarbonate and 72 ml of a saturated aqueous solution of sodium chloride in this order, subsequently dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The operation of adding 5 ml of toluene to the obtained concentration residue and concentrating the resultant under reduced pressure was repeated five times to obtain crude ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate.

To a solution of 6.70 g of the obtained crude ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate in 235 ml of dehydrated dichloromethane, 8.8 ml (51 mmol) of DIPEA was added at room temperature in an argon atmosphere, and then, a solution of 3.79 g (12.8 mmol) of bis(trichloromethyl)carbonate in 38 ml of dehydrated dichloromethane was added dropwise at −78° C. and stirred at the same temperature as above for 3 hours. At each point in time of 1 hour, 2 hours, and 2.6 hours after the start of this reaction, 1.0 ml (5.7 mmol) of DIPEA was added thereto.

After the completion of the reaction, 150 ml of a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred while the temperature was raised to room temperature for a while. After separation into an aqueous layer and an organic layer, the aqueous layer was subjected to extraction with 130 ml of dichloromethane twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=78:22 to 57:43 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. n-Hexane was added to the obtained concentration residue and ultrasonicated. After cooling in a refrigerator, the deposited solid was filtered and dried under reduced pressure to obtain 3.51 g of the title compound (yield: 46% [2 steps]) as a white solid.

Mass spectrum (CI, m/z): 441 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.83-9.65 (m, 1H), 4.84 (s, 2H), 4.49-4.37 (m, 2H), 2.54-2.43 (m, 2H), 2.31-2.21 (m, 2H), 1.95-1.83 (m, 2H), 1.71-1.58 (m, 6H), 1.35 (t, J=7.1 Hz, 3H), 0.13-0.08 (m, 9H).

Reference Example 4 5-tert-Butyl 1-ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]pyrrolo[3,4-c]pyrazole-1,5(4H,6H)-dicarboxylate

To a solution of 24.52 g (142 mmol) of 1-(trimethylsilyl)cyclobutanecarboxylic acid synthesized in the similar manner as in Reference Example 1 in 180 ml of dehydrated dichloromethane, 0.55 ml (7.1 mmol) of DMF and 12.2 ml (142 mmol) of oxalyl chloride were added dropwise at 0° C. in an argon atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure (hot water bath temperature: 30° C.) to obtain a concentration residue.

To a solution of 15.39 g (47.4 mmol) of 5-tert-butyl 1-ethyl 3-amino-6,6-dimethylpyrrolo[3,4-c]pyrazole-1,5(4H,6H)-dicarboxylate [synthesized according to the method described in Journal of Medicinal Chemistry 2012, 55 (10), 4728-4739] and 40.6 ml (238 mmol) of DIPEA in 180 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 120 ml of dehydrated dichloromethane was added dropwise at 0° C. in an argon atmosphere and stirred at the same temperature as above for 20 hours.

After the completion of the reaction, the reaction solution was poured to 800 ml of a 5% aqueous potassium bisulfate solution, stirred, and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with 250 ml of dichloromethane twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=91:9 to 70:30 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 14.6 g of the title compound (yield: 64%) as a white foam.

Mass spectrum (EI, m/z): 478 [M]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 10.32-10.20 (m, 1H), 4.46-4.32 (m, 4H), 2.48-2.39 (m, 2H), 2.24-2.14 (m, 2H), 1.84-1.68 (m, 8H), 1.52-1.40 (m, 9H), 1.32 (t, J=7.1 Hz, 3H), 0.07 (s, 9H).

Reference Example 5 Ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate

To a solution of 10.02 g (20.9 mmol) of 5-tert-butyl 1-ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]pyrrolo[3,4-c]pyrazole-1,5(4H,6H)-dicarboxylate synthesized in the similar manner as in Reference Example 4 in 100 ml of dehydrated dichloromethane, 7.26 ml (62.7 mmol) of 2,6-lutidine and 11.3 ml (62.7 mmol) of trimethylsilyl trifluoromethanesulfonate were added dropwise at 0° C. in an argon atmosphere and stirred at the same temperature as above for 1.5 hours.

After the completion of the reaction, 60 ml of a saturated aqueous solution of sodium bicarbonate and 60 ml of dichloromethane were added to the reaction solution. After separation into an aqueous layer and an organic layer, the aqueous layer was subjected to extraction with 60 ml of dichloromethane twice. All of the obtained organic layers were washed with 60 ml of a saturated aqueous solution of sodium bicarbonate and 60 ml of a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The operation of adding toluene to the obtained concentration residue and concentrating it under reduced pressure was repeated three times to obtain 7.43 g of the title compound (yield: 94%) as a pale yellow solid.

Mass spectrum (EI, m/z): 378 [M]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 10.03 (s, 1H), 4.37 (q, J=7.1 Hz, 2H), 3.85 (s, 2H), 2.48-2.38 (m, 2H), 2.23-2.12 (m, 2H), 1.85-1.72 (m, 2H), 1.41 (s, 6H), 1.31 (t, J=7.1 Hz, 3H), 0.06 (s, 9H).

Reference Example 6 5-tert-Butyl 2-ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]pyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate

To a solution of 1.05 g (6.63 mmol) of 1-(trimethylsilyl)cyclopropanecarboxylic acid [synthesized according to the method described in J. Org. Chem., 1982, 47 (5), 893-895] in 20 ml of dehydrated dichloromethane, 0.70 ml (8.2 mmol) of oxalyl chloride and 0.020 ml (0.26 mmol) of DMF were added at 0° C. in a nitrogen atmosphere and stirred at the same temperature as above for 3 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure (hot water bath temperature: 25° C.) to obtain a concentration residue.

To a solution of the obtained concentration residue in 15 ml of dehydrated dichloromethane, 1.80 ml (10.3 mmol) of DIPEA and 839 mg (2.59 mmol) of 5-tert-butyl 2-ethyl 3-amino-6,6-dimethylpyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate [synthesized according to the method described in Journal of Medicinal Chemistry 2012, 55 (10), 4728-4739] were added at 0° C. in a nitrogen atmosphere and stirred at the same temperature as above for 20.5 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 75:25 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 1.19 g of the title compound (containing impurities) as a pale yellow foam.

Mass spectrum (CI, m/z): 465 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 10.09 & 9.92 (s, total 1H), 4.70-4.46 (m, 4H), 1.72 (s, 3H), 1.65 (s, 3H), 1.54-1.44 (m, 12H), 1.15-1.07 (m, 2H), 0.84-0.78 (m, 2H), 0.17-0.07 (m, 9H).

Reference Example 7 Ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate hydrochloride

To a solution of 1.19 g of 5-tert-butyl 2-ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]pyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate (containing impurities) synthesized in the similar manner as in Reference Example 6 in 20 ml of ethyl acetate, 4.0 ml (16 mmol) of 4 N hydrogen chloride/ethyl acetate was added at room temperature in a nitrogen atmosphere and stirred at the same temperature as above for 6.5 hours. Then, 2.0 ml (8.0 mmol) of 4 N hydrogen chloride/ethyl acetate was added thereto and further stirred at room temperature for 14.5 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and the obtained concentration residue was suspended in diisopropyl ether and stirred at room temperature. Insoluble matter was collected by filtration, and the obtained solid was washed by sousing with diisopropyl ether and then dried under reduced pressure to obtain 0.91 g of the title compound (yield: 88% [2 steps]) as a white solid.

Mass spectrum (CI, m/z): 365 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.99 (br s, 2H), 9.91 (s, 1H), 4.51-4.39 (m, 4H), 1.63 (s, 6H), 1.35 (t, J=7.2 Hz, 3H), 1.08 (dd, J=4.2, 6.0 Hz, 2H), 0.87 (dd, J=4.2, 6.0 Hz, 2H), 0.08 (s, 9H).

Reference Example 8 2-Methyl-2-(trimethylsilyl)propanoic acid

To 100 ml of dehydrated THF, 200 ml (400 mmol) of 2 M lithium diisopropylamide/THF solution was added in an argon atmosphere, and subsequently, 4.7 ml (51 mmol) of isobutanoic acid was added dropwise at 0° C. and then stirred at room temperature for 4 hours. 10 ml (58 mmol) of hexamethylphosphoric acid triamide was added thereto, and then, 29 ml (230 mmol) of chlorotrimethylsilane was added thereto dropwise at −78° C. and stirred for 24 hours while the temperature was gradually raised to room temperature.

After the completion of the reaction, 25 ml of methanol and 50 ml of water were added to the reaction solution. Subsequently, the solution was rendered acidic by adding 2 N hydrochloric acid, followed by extraction with diethyl ether. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was dissolved in a 2 N aqueous sodium hydroxide solution and washed with ethyl acetate. After separation into an aqueous layer and an organic layer, the aqueous layer was rendered acidic by adding 1 N hydrochloric acid, followed by extraction with ethyl acetate. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was suspended in n-hexane, and after ultrasonication, insoluble matter was collected by filtration. The filtrate was concentrated under reduced pressure, the obtained concentration residue was subjected to silica gel column chromatography (elution solvent: 1,2-dichloroethane:methanol=100:0 to 99:1 (V/V)), and a fraction containing the compound of interest and the aforementioned solid collected by filtration were combined, concentrated under reduced pressure, and dried under reduced pressure to obtain 2.66 g of the title compound (yield: 32%) as a white solid.

Mass spectrum (CI, m/z): 161 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 1.22 (s, 6H), 0.08 (s, 9H).

Reference Example 9 5-tert-Butyl 1-ethyl 6,6-dimethyl-3-[2-methyl-2-(trimethylsilyl)propanamido]pyrrolo[3,4-c]pyrazole-1,5(4H,6H)-dicarboxylate

To a solution of 1.30 g (8.11 mmol) of 2-methyl-2-(trimethylsilyl)propanoic acid synthesized in the similar manner as in Reference Example 8 in 25 ml of dehydrated dichloromethane, 0.85 ml (9.9 mmol) of oxalyl chloride and 0.040 ml (0.52 mmol) of DMF were added in this order at 0° C. in a nitrogen atmosphere and stirred at the same temperature as above for 3.5 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure (hot water bath temperature: 25° C.) to obtain a concentration residue.

To a solution of the obtained concentration residue in 15 ml of dehydrated dichloromethane, 2.30 ml (13.2 mmol) of DIPEA and 1.08 g (3.33 mmol) of 5-tert-butyl 1-ethyl 3-amino-6,6-dimethylpyrrolo[3,4-c]pyrazole-1,5(4H,6H)-dicarboxylate [synthesized according to the method described in Journal of Medicinal Chemistry 2012, 55 (10), 4728-4739] were added in this order at 0° C. in a nitrogen atmosphere and stirred at the same temperature as above for 17.5 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred, followed by extraction with dichloromethane three times. All of the organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=93:7 to 80:20 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 1.28 g of the title compound (yield: 82%) as a pale yellow foam.

Mass spectrum (CI, m/z): 467 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.87-7.74 (m, 1H), 4.60-4.47 (m, 4H), 1.84 & 1.78 (s, total 6H), 1.55-1.48 (m, 9H), 1.47 (t, J=7.2 Hz, 3H), 1.31-1.25 (m, 6H), 0.10-0.04 (m, 9H).

Reference Example 10 1-(Ethyldimethylsilyl)cyclobutanecarboxylic acid

To 200 ml of dehydrated THF, 214 ml (428 mmol) of 2 M lithium diisopropylamide/THF solution was added in an argon atmosphere, and then, 10.7 ml (112 mmol) of cyclobutanecarboxylic acid was added dropwise under cooling in ice water and stirred while the temperature was raised to room temperature for a while. Subsequently, 20 ml (120 mmol) of hexamethylphosphoric acid triamide was added. After cooling in a dry ice/ethanol coolant, 67.6 ml (485 mmol) of chloro(ethyl)dimethylsilane was added dropwise at −75° C. to −69° C. and stirred overnight at a temperature of −60° C. or lower.

After the completion of the reaction, 67 ml of methanol and subsequently 134 ml of cold water were added dropwise to the reaction solution and then brought to room temperature. 240 ml of 2 N hydrochloric acid was added for acidity (pH 2.0), and 200 ml of diethyl ether was added thereto and then the aqueous layer and the organic layer were separated. The obtained organic layer was washed with 250 ml of a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. 41 ml of a 2 N aqueous sodium hydroxide solution was added to the obtained concentration residue and washed with 250 ml of n-hexane. The aqueous layer was rendered acidic (pH 2.0) again by adding 82 ml of 1 N hydrochloric acid. This solution was subjected to extraction with 250 ml of ethyl acetate, and the organic layer was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 11.7 g of the title compound (yield: 59%) as a white solid.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 11.71 (br s, 1H), 2.44-2.33 (m, 2H), 2.19-2.08 (m, 2H), 1.91-1.73 (m, 2H), 0.92 (t, J=7.9 Hz, 3H), 0.55 (q, J=7.9 Hz, 2H), 0.05 (s, 6H).

Reference Example 11 5-tert-Butyl 2-ethyl 3-[1-(ethyldimethylsilyl)cyclobutanecarboxamido]-6,6-dimethylpyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate

To a solution of 11.7 g (62.8 mmol) of 1-(ethyldimethylsilyl)cyclobutanecarboxylic acid synthesized in the similar manner as in Reference Example 10 in 81 ml of dehydrated dichloromethane, 5.3 ml (62 mmol) of oxalyl chloride and 0.24 ml (3.1 mmol) of DMF were added in this order under cooling in ice water in an argon atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure at room temperature to obtain a concentration residue.

To a solution of 6.73 g (20.7 mmol) of 5-tert-butyl 2-ethyl 3-amino-6,6-dimethylpyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate [synthesized according to the method described in Journal of Medicinal Chemistry 2012, 55 (10), 4728-4739] and 18 ml (100 mmol) of DIPEA in 94 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 5 ml of dehydrated dichloromethane was added dropwise under cooling in ice water in a nitrogen atmosphere and stirred at the same temperature as above for 16 hours.

After the completion of the reaction, 350 ml of a 5% aqueous potassium bisulfate solution was added to the reaction solution and separated into an aqueous layer and an organic layer, and then, the aqueous layer was subjected to extraction with 150 ml of dichloromethane twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate and then filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=86:14 to 53:47 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 7.51 g of the title compound (yield: 74%) as a pale yellow oil.

Mass spectrum (DUIS, m/z): 493 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.82-9.69 (m, 1H), 4.51-4.36 (m, 4H), 2.49-2.42 (m, 2H), 2.32-2.23 (m, 2H), 1.95-1.84 (m, 2H), 1.62-1.55 (m, 6H), 1.49-1.42 (m, 9H), 1.38-1.31 (m, 3H), 0.91 (t, J=7.9 Hz, 3H), 0.57 (q, J=7.9 Hz, 2H), 0.09 (s, 6H).

Reference Example 12 Ethyl 3-[1-(ethyldimethylsilyl)cyclobutanecarboxamido]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate

To a solution of 7.27 g (14.8 mmol) of 5-tert-butyl 2-ethyl 3-[1-(ethyldimethylsilyl)cyclobutanecarboxamido]-6,6-dimethylpyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate synthesized in the similar manner as in Reference Example 11 in 70 ml of dehydrated dichloromethane, 5.1 ml (44 mmol) of 2,6-lutidine and 7.8 ml (43 mmol) of trimethylsilyl trifluoromethanesulfonate were added dropwise in this order under ice cooling in an argon atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, 57 ml of a saturated aqueous solution of sodium bicarbonate and 57 ml of dichloromethane were added to the reaction solution, and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with 60 ml of dichloromethane twice, all of the obtained organic layers were washed with 60 ml of a saturated aqueous solution of sodium bicarbonate and 60 ml of a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The operation of adding toluene to the obtained concentration residue and concentrating the resultant under reduced pressure was performed five times to obtain 5.92 g of the title compound (containing impurities) as a yellow oil.

Mass spectrum (DUIS, m/z): 393 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.68 (s, 1H), 4.39 (q, J=7.0 Hz, 2H), 3.92 (s, 2H), 2.48-2.40 (m, 2H), 2.29-2.22 (m, 2H), 1.93-1.82 (m, 2H), 1.33 (t, J=7.0 Hz, 3H), 1.29 (s, 6H), 0.91 (t, J=8.1 Hz, 3H), 0.56 (q, J=8.1 Hz, 2H), 0.08 (s, 6H).

Reference Example 13 Ethyl 5-(chlorocarbonyl)-3-[1-(ethyldimethylsilyl)cyclobutanecarboxamido]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate

To a solution of 5.92 g of ethyl 3-[1-(ethyldimethylsilyl)cyclobutanecarboxamido]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate (containing impurities) synthesized in the similar manner as in Reference Example 12 by using 7.27 g (14.8 mmol) of 5-tert-butyl 2-ethyl 3-[1-(ethyldimethylsilyl)cyclobutanecarboxamido]-6,6-dimethylpyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate synthesized in the similar manner as in Reference Example 11 in 200 ml of dehydrated dichloromethane, 7.3 ml (43 mmol) of DIPEA was added at room temperature in an argon atmosphere, and then, a solution of 3.24 g (10.9 mmol) of bis(trichloromethyl)carbonate in 33 ml of dehydrated dichloromethane was added dropwise at −60° C. or lower and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, 130 ml of a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, and the temperature was raised to room temperature for a while with stirring. After separation into an aqueous layer and an organic layer, the aqueous layer was subjected to extraction with 100 ml of dichloromethane twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=78:22 to 57:43 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. n-Hexane was added to the concentration residue and concentrated again under reduced pressure to obtain 5.13 g of the title compound (yield: 76% [2 steps]) as a white solid.

Mass spectrum (CI, m/z): 455 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.85-9.76 (m, 1H), 4.88-4.81 & 4.53-4.48 (m, total 2H), 4.44 (q, J=7.1 Hz, 2H), 2.55-2.44 (m, 2H), 2.35-2.24 (m, 2H), 1.96-1.85 (m, 2H), 1.69-1.61 (m, 6H), 1.34 (t, J=7.1 Hz, 3H), 0.92 (t, J=7.9 Hz, 3H), 0.58 (q, J=7.9 Hz, 2H), 0.13-0.07 (m, 6H).

Reference Example 14 2-(Ethyldimethylsilyl)-2-methylpropanoic acid

To 100 ml of dehydrated THF, 100 ml (200 mmol) of 2 M lithium diisopropylamide/THF solution was added in an argon atmosphere, and then, 4.7 ml (51 mmol) of isobutanoic acid was added dropwise at 0° C. and stirred for 4 hours after the temperature was raised to room temperature. Subsequently, 10 ml (58 mmol) of hexamethylphosphoric acid triamide was added thereto, and then, 32 ml (230 mmol) of chloro(ethyl)dimethylsilane was added thereto dropwise at −78° C. After the completion of the dropwise addition, the resultant was stirred for 1 day while the temperature was raised to room temperature for a while.

After the completion of the reaction, 25 ml of methanol and subsequently 50 ml of water were added under cooling in ice water. Then, 2 N hydrochloric acid was added for acidity, followed by extraction with diethyl ether. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. A 2 N aqueous sodium hydroxide solution was added to the concentration residue, and it was washed with ethyl acetate. Subsequently, the aqueous layer was rendered acidic by adding a 1 N aqueous hydrochloric acid solution, followed by extraction with ethyl acetate. The obtained organic layer was dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: 1,2-dichloroethane:methanol=100:0 to 99:1 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 2.24 g of the title compound (yield: 25%) as a white solid.

Mass spectrum (CI, m/z): 175 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 11.57 (br s, 1H), 1.23 (s, 6H), 0.95 (t, J=8.0 Hz, 3H), 0.62 (q, J=8.0 Hz, 2H), 0.06 (s, 6H).

Reference Example 15 5-tert-Butyl 1-ethyl 3-[2-(ethyldimethylsilyl)-2-methylpropanamido]-6,6-dimethylpyrrolo[3,4-c]pyrazole-1,5(4H,6H)-dicarboxylate

To a solution of 4.7 g (27 mmol) of 2-(ethyldimethylsilyl)-2-methylpropanoic acid synthesized in the similar manner as in Reference Example 14 in 40 ml of dehydrated dichloromethane, 2.3 ml (27 mmol) of oxalyl chloride was added dropwise at 0° C. in an argon atmosphere and stirred at the same temperature as above for 10 minutes. Subsequently, 0.10 ml (1.3 mmol) of DMF was added at 0° C. and stirred at the same temperature as above for 4 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure at room temperature to obtain a concentration residue.

To a solution of 2.9 g (8.9 mmol) of 5-tert-butyl 1-ethyl 3-amino-6,6-dimethylpyrrolo[3,4-c]pyrazole-1,5(4H,6H)-dicarboxylate [synthesized according to the method described in Journal of Medicinal Chemistry 2012, 55 (10), 4728-4739] in 10 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 20 ml of dehydrated dichloromethane was added dropwise at 0° C. in an argon atmosphere, and subsequently, 7.9 ml (45 mmol) of DIPEA was added and stirred at 0° C. for 24 hours.

After the completion of the reaction, water was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=98:2 to 80:20 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 3.18 g of the title compound (yield: 74%) as a pale yellow oil.

Mass spectrum (CI, m/z): 481 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.88-7.73 (m, 1H), 4.62-4.46 (m, 4H), 1.87-1.75 (m, 6H), 1.55-1.41 (m, 12H), 1.31-1.26 (m, 6H), 0.99-0.88 (m, 3H), 0.66-0.53 (m, 2H), 0.09-0.02 (m, 6H).

Reference Example 16 Ethyl 3-[2-(ethyldimethylsilyl)-2-methylpropanamido]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-1 (4H)-carboxylate

To a solution of 3.18 g (6.62 mmol) of 5-tert-butyl 1-ethyl 3-[2-(ethyldimethylsilyl)-2-methylpropanamido]-6,6-dimethylpyrrolo[3,4-c]pyrazole-1,5(4H,6H)-dicarboxylate synthesized in the similar manner as in Reference Example 15 in 30 ml of dehydrated dichloromethane, 2.3 ml (20 mmol) of 2,6-lutidine and 3.6 ml (20 mmol) of trimethylsilyl trifluoromethanesulfonate were added dropwise in this order at 0° C. in an argon atmosphere and stirred at the same temperature as above for 1 hour.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. Toluene was added to the residue, and then, concentration under reduced pressure was performed to obtain 2.44 g of the title compound (yield: 97%) as a pale yellow solid.

Mass spectrum (CI, m/z): 381 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.77 (s, 1H), 4.50 (q, J=7.2 Hz, 2H), 4.15 (s, 2H), 1.55 (s, 6H), 1.46 (t, J=7.2 Hz, 3H), 1.32-1.25 (m, 6H), 0.93 (t, J=8.0 Hz, 3H), 0.60 (q, J=8.0 Hz, 2H), 0.05 (s, 6H).

Reference Example 17 (S)-2-[(2-Methoxypropan-2-yl)oxy]-1-phenylethanol

To a solution of 664 mg (2.63 mmol) of (S)-2-[(tert-butyldimethylsilyl)oxy]-2-phenylethanol [synthesized according to the method described in Angew. Chem. Int. Ed., 2012, 51 (31), 7825-7829] in 15 ml of dichloromethane, 0.33 ml (3.5 mmol) of 2-methoxy-1-propene and 68.3 mg (0.272 mmol) of pyridinium p-toluenesulfonate were added at 0° C. in a nitrogen atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred, followed by extraction with dichloromethane twice. All of the organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=98:2 to 97:3 (V/V)), and a fraction containing (S)-3,3,8,8,9,9-hexamethyl-6-phenyl-2,4,7-trioxa-8-siladecane was concentrated under reduced pressure and dried under reduced pressure to obtain a concentration residue.

To a solution of 347 mg of the obtained concentration residue in 10 ml of THF, 428 mg (1.64 mmol) of tetrabutylammonium fluoride was added at 0° C. in a nitrogen atmosphere and stirred at the same temperature as above for 3.5 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred, followed by extraction with an ethyl acetate/n-hexane mixed solvent twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 85:15 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 160 mg of the title compound (yield: 29% [2 steps]) as a colorless oil.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.43-7.27 (m, 5H), 4.89-4.83 (m, 1H), 3.59 (dd, J=3.2, 9.8 Hz, 1H), 3.45 (dd, J=9.0, 9.8 Hz, 1H), 3.19 (s, 3H), 2.82 (d, J=2.4 Hz, 1H), 1.38 (s, 3H), 1.37 (s, 3H).

Reference Example 18 (S)-2,5-Dioxopyrrolidin-1-yl {2-[(2-methoxypropan-2-yl)oxy]-1-phenylethyl}carbonate

To a solution of 157 mg (0.747 mmol) of (S)-2-[(2-methoxypropan-2-yl)oxy]-1-phenylethanol synthesized in the similar manner as in Reference Example 17 in 4 ml of dehydrated acetonitrile, 0.16 ml (1.2 mmol) of triethylamine and 233 mg (0.908 mmol) of N,N′-disuccinimidyl carbonate were added at room temperature in a nitrogen atmosphere and stirred at the same temperature as above for 6 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, and it was washed with water. After separation into an aqueous layer and an organic layer, the aqueous layer was subjected to extraction with ethyl acetate twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 65:35 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 190 mg of the title compound (yield: 72%) as a colorless oil.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.42-7.33 (m, 5H), 5.86 (dd, J=3.4, 8.8 Hz, 1H), 3.83 (dd, J=8.8, 11.0 Hz, 1H), 3.64 (dd, J=3.4, 11.0 Hz, 1H), 3.20 (s, 3H), 2.81 (s, 4H), 1.38 (s, 3H), 1.34 (s, 3H).

Reference Example 19 Ethyl 4-(benzyloxy)-3-phenylbutanoate

To a solution of 8.9 mg (0.023 mmol) of bis(acetonitrile)(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate in 3 ml of 1,4-dioxane/0.3 ml of water, 23 mg (0.41 mmol) of potassium hydroxide, 128 mg (1.05 mmol) of phenylboronic acid, and 120 mg (0.545 mmol) of (E)-ethyl 4-(benzyloxy)-2-butenoate [synthesized according to the method described in Tetrahedron Lett., 1982, 37, 9033-9036] were added in this order with stirring at room temperature in an argon atmosphere, stirred at the same temperature as above for 30 minutes, and then stirred at 60° C. for 6 hours.

After the completion of the reaction, water was added to the reaction solution, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=95:5 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 160 mg of the title compound (yield: 98%) as a pale yellow oil.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.36-7.18 (m, 10H), 4.45 (s, 2H), 3.97-3.89 (m, 2H), 3.59-3.52 (m, 2H), 3.39-3.33 (m, 1H), 2.81 (dd, J=6.3, 15.6 Hz, 1H), 2.59 (dd, J=8.5, 15.6 Hz, 1H), 1.04 (t, J=7.1 Hz, 3H).

Reference Example 20 Ethyl 6,6-dimethyl-5-(3-oxo-3-phenylpropanoyl)-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate and (Z)-ethyl 5-(3-hydroxy-3-phenylacryloyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate as tautomer

To a solution of 487 mg (2.39 mmol) of 3-oxo-3-phenylpropanoic acid [synthesized according to the method described in Chem. Pharm. Bull., 29 (10), 2762 (1981)] and 10 μl (0.13 mmol) of DMF in 5 ml of dehydrated dichloromethane, 205 μl (2.39 mmol) of oxalyl chloride was added dropwise with stirring at 0° C. in an argon atmosphere and stirred for 1.5 hours after the temperature was raised to room temperature.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure at room temperature to obtain a concentration residue.

To a solution of 299 mg (0.790 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.70 ml (4.1 mmol) of DIPEA in 5 ml of 1,2-dichloroethane, a solution of the obtained concentration residue in 5 ml of 1,2-dichloroethane was added dropwise with stirring at room temperature in an argon atmosphere and stirred at the same temperature as above for 5 hours.

After the completion of the reaction, 5 ml of 2-propanol was added and stirred at room temperature for 14 hours, and then, the reaction solution was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=87:13 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 293 mg of the title compound (yield: 71%) (containing the tautomer) as a pale yellow solid.

Mass spectrum (DUIS, m/z): 525 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 15.71 (s, 0.3H), 9.79 (s, 0.3H), 9.75 (s, 0.7H), 8.01-7.42 (m, total 5H), 5.82 (s, 0.3H), 4.85 (s, 0.6H), 4.78 (s, 1.4H), 4.47-4.38 (m, total 2H), 4.18 (s, 1.4H), 2.57-2.41 (m, total 2H), 2.33-2.12 (m, total 2H), 1.93-1.81 (m, total 2H), 1.75 & 1.64 (s, total 6H), 1.38-1.31 (m, total 3H), 0.11 & 0.08 (s, total 9H).

Reference Example 21 (R)-Methyl 3-amino-3-phenylpropanoate hydrochloride

To a solution of 2.01 g (12.2 mmol) of (R)-3-amino-3-phenylpropanoic acid [purchased from Shanghai HC Biotech Co., Ltd.] in 100 ml of dehydrated methanol, 1.32 ml (18.2 mmol) of thionyl chloride was added dropwise with stirring at room temperature in a nitrogen atmosphere and then stirred at the same temperature as above for 24 hours. Then, the temperature was raised to 65° C., and the resultant was stirred for 9.5 hours.

After standing to cool, the reaction solution was concentrated under reduced pressure, diethyl ether was added to the obtained concentration residue and ultrasonicated, and the deposited solid was collected by filtration and dried under reduced pressure to obtain 2.55 g of the title compound (yield: 97%) as a white solid.

Mass spectrum (DUIS, m/z): 180 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 8.67 (br s, 3H), 7.57-7.50 (m, 2H), 7.45-7.36 (m, 3H), 4.58 (dd, J=6.0, 8.6 Hz, 1H), 3.35 (br s, 3H), 3.20 (dd, J=6.0, 16.3 Hz, 1H), 3.00 (dd, J=8.6, 16.3 Hz, 1H).

Reference Example 22 (R)-Methyl 3-phenyl-3-(2,2,2-trifluoroacetamido)propanoate

To a solution of 2.55 g (11.8 mmol) of (R)-methyl 3-amino-3-phenylpropanoate hydrochloride synthesized in the similar manner as in Reference Example 21 in 50 ml of dichloromethane, 10.5 ml (60.3 mmol) of DIPEA and 1.75 ml (12.4 mmol) of trifluoroacetic anhydride were added dropwise in this order with stirring at 0° C. in an argon atmosphere, stirred at the same temperature as above for 2 hours, and further stirred overnight at room temperature.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. Ethyl acetate was added to the concentration residue, washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=91:9 to 70:30 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 2.75 g of the title compound (yield: 85%) as a white solid.

Mass spectrum (DUIS, m/z): 276 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.80-7.64 (m, 1H), 7.39-7.25 (m, 5H), 5.46-5.39 (m, 1H), 3.65 (s, 3H), 3.00 (dd, J=5.5, 16.2 Hz, 1H), 2.93 (dd, J=5.5, 16.2 Hz, 1H).

Reference Example 23 (R)-4-Amino-2-methyl-4-phenylbutan-2-ol

To a solution of 506 mg (1.84 mmol) of (R)-methyl 3-phenyl-3-(2,2,2-trifluoroacetamido)propanoate synthesized in the similar manner as in Reference Example 22 in 5 ml of dehydrated THF, 6.60 ml (9.24 mmol) of 1.4 M methyl magnesium bromide/THF solution was added dropwise with stirring at room temperature in an argon atmosphere and stirred at room temperature for 3.5 hours.

After the completion of the reaction, 10 ml of a saturated aqueous solution of ammonium chloride was added dropwise to the reaction solution under ice cooling, brought back to room temperature, and stirred for a while. Dichloromethane and water, and further an aqueous solution of dilute sodium hydroxide were added to the reaction solution to adjust the pH of the aqueous layer to 10, followed by separation into an aqueous layer and an organic layer. The aqueous layer was subjected to extraction with dichloromethane, all of the obtained organic layers were dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (DNH silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing (R)-2,2,2-trifluoro-N-(3-hydroxy-3-methyl-1-phenylbutyl)acetamide was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 427 mg of the obtained concentration residue in 5 ml of ethanol, 64.6 mg (1.71 mmol) of sodium borohydride was added in several divided portions at room temperature and then stirred at room temperature for 14 hours. 77.0 mg (2.04 mmol) of sodium borohydride was further added in several divided portions, stirred at room temperature for 2 hours, and then stirred at 75° C. for 2 hours.

After the completion of the reaction, the reaction solution was cooled in ice, and 10 ml of a saturated aqueous solution of ammonium chloride was added thereto dropwise and then stirred at room temperature. Dichloromethane and water were added thereto, and an aqueous solution of dilute sodium hydroxide was added thereto to adjust the pH of the aqueous layer to 10, followed by separation into an aqueous layer and an organic layer. The aqueous layer was subjected to extraction with dichloromethane, all of the obtained organic layers were dried over anhydrous sodium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The concentration residue was subjected to silica gel column chromatography (DNH silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 160 mg of the title compound (yield: 49%) as a colorless oil.

Mass spectrum (DUIS, m/z): 180 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.37-7.26 (m, 4H), 7.21-7.15 (m, 1H), 4.05 (dd, J=2.8, 10.7 Hz, 1H), 1.66 (dd, J=10.7, 14.0 Hz, 1H), 1.52 (dd, J=2.8, 14.0 Hz, 1H), 1.22 (s, 3H), 1.10 (s, 3H).

Reference Example 24 (S)-tert-Butyl [2-(difluoromethoxy)-1-phenylethyl]carbamate

To a solution of 1.00 g (4.21 mmol) of (S)-tert-butyl (2-hydroxy-1-phenylethyl)carbamate [purchased from Novo Chemy Ltd.] in 30 ml of dehydrated acetonitrile, 165 mg (0.866 mmol) of copper(I) iodide was added at room temperature in an argon atmosphere and stirred at the same temperature as above for 30 minutes. Subsequently, a solution of 0.87 ml (8.4 mmol) of 2-(fluorosulfonyl)difluoroacetic acid in 10 ml of dehydrated acetonitrile was dividedly added (1 ml each) at 45° C. over 40 minutes and stirred at the same temperature as above for 1 hour.

After the completion of the reaction, the reaction solution allowed to cool to room temperature was concentrated under reduced pressure. Water and ethyl acetate were added to the obtained concentration residue, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with water, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=95:5 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained concentration residue was subjected again to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=95:5 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 213 mg of the title compound (yield: 18%) as a yellow solid.

Mass spectrum (CI, m/z): 288 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.55 (d, J=8.7 Hz, 1H), 7.37-7.24 (m, 5H), 6.67 (t, J=75.9 Hz, 1H), 4.83-4.73 (m, 1H), 3.95-3.86 (m, 2H), 1.42-1.23 (m, 9H).

Reference Example 25 (S)-2-(Difluoromethoxy)-1-phenylethanamine trifluoroacetate

To a solution of 210 mg (0.731 mmol) of (S)-tert-butyl [2-(difluoromethoxy)-1-phenylethyl]carbamate synthesized in the similar manner as in Reference Example 24 in 4 ml of dehydrated dichloromethane, 1 ml of trifluoroacetic acid was added at room temperature in an argon atmosphere and stirred at the same temperature as above for 2 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure and dried under reduced pressure to obtain 210 mg of the title compound (yield: 95%) as a yellow oil.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 8.59 (br s, 3H), 7.54-7.40 (m, 5H), 6.76 (t, J=74.8 Hz, 1H), 4.70-4.59 (m, 1H), 4.19-4.11 (m, 2H).

Reference Example 26 (S)-2-Ethoxy-1-phenylethanamine

To a solution of 1.40 g (10.2 mmol) of (S)-2-amino-2-phenylethanol and 3.0 ml (15 mmol) of 1,4,7,10,13-pentaoxacyclopentadecane in 10 ml of dehydrated THF, 481 mg (11.0 mmol) of 55% sodium hydride was dividedly added with stirring at room temperature in an argon atmosphere and stirred at the same temperature as above until foaming settled. Subsequently, 0.82 ml (10 mmol) of ethyl iodide was added dropwise at room temperature and stirred at the same temperature as above for 24 hours.

After the completion of the reaction, water and diethyl ether were added to the reaction solution and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with diethyl ether, then all of the organic layers were washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (DNH silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 1.17 g of the title compound (yield: 69%) as a pale yellow oil.

Mass spectrum (CI, m/z): 166 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.39-7.33 (m, 2H), 7.33-7.25 (m, 2H), 7.25-7.19 (m, 1H), 4.01 (dd, J=4.9, 8.0 Hz, 1H), 3.53-3.35 (m, 3H), 3.28 (dd, J=8.0, 9.3 Hz, 1H), 1.82 (br s, 2H), 1.09 (t, J=7.0 Hz, 3H).

Reference Example 27 (R)-3-Methoxy-1-phenylpropan-1-amine

To a solution of 1.53 g (10.1 mmol) of (R)-3-amino-3-phenylpropan-1-ol [purchased from Ark Pharm, Inc.] and 3.0 ml (15 mmol) of 1,4,7,10,13-pentaoxacyclopentadecane in 10 ml of dehydrated THF, 473 mg (10.9 mmol) of 55% sodium hydride was dividedly added with stirring at room temperature in an argon atmosphere and stirred at the same temperature as above until foaming settled. Subsequently, 0.62 ml (10 mmol) of methyl iodide was added thereto dropwise at 0° C. and then stirred at room temperature for 17 hours.

After the completion of the reaction, water and diethyl ether were added to the reaction solution and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with diethyl ether, then all of the organic layers were washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (DNH silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 1.49 g of the title compound (yield: 89%) as a colorless oil.

Mass spectrum (CI, m/z): 166 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.35-7.26 (m, 4H), 7.24-7.15 (m, 1H), 3.85 (dd, J=6.4, 7.4 Hz, 1H), 3.38-3.20 (m, 2H), 3.19 (s, 3H), 1.93-1.63 (m, 4H).

Reference Example 28 2-(Benzo[d][1,3]dioxol-4-yl)-2-[(tert-butoxycarbonyl)amino]acetic acid

To a solution of 7.09 g (47.2 mmol) of benzo[d][1,3]dioxole-4-carbaldehyde in 15 ml of methanol, 67.5 ml (472 mmol) of 7 M aqueous ammonia solution/methanol solution was gradually added at room temperature and then stirred at room temperature for 18 minutes. The reaction solution was cooled in ice water, and 14.1 ml (113 mmol) of trimethylsilane carbonitrile was added dropwise. After the completion of the dropwise addition, the resultant was stirred overnight at room temperature.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To 9.30 g of the obtained concentration residue, 17 ml of acetic acid and 66.7 ml (776 mmol) of concentrated hydrochloric acid were added and stirred for 9 hours while heated to reflux.

After standing to cool, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To 8.33 g of the obtained concentration residue, 35.2 ml (141 mmol) of a 4 N aqueous sodium hydroxide solution, 65 ml of 1,4-dioxane, and 14.7 ml (64.1 mmol) of di-tert-butyl dicarbonate were added in this order at room temperature and stirred at room temperature.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, 100 ml of dichloromethane was added thereto, and then, the pH was adjusted to 1.75 by using concentrated hydrochloric acid. Methanol was added thereto until insoluble matter was dissolved, and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with 100 ml of dichloromethane twice, all of the obtained organic layers were dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: ethyl acetate), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained residue was subjected again to silica gel column chromatography (elution solvent: ethyl acetate), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 10.22 g of the title compound (yield: 73% [3 steps]) as a black viscous liquid.

Mass spectrum (DUIS, m/z): 296 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 13.24-12.32 (m, 1H), 7.48 (d, J=8.5 Hz, 1H), 6.88-6.77 (m, 3H), 6.04-6.01 (m, 2H), 5.22 (d, J=8.5 Hz, 1H), 1.38 (s, 9H).

Reference Example 29 Methyl 2-(benzo[d][1,31]dioxol-4-yl)-2-[(tert-butoxycarbonyl)amino]acetate

To a solution of 3.93 g (13.3 mmol) of 2-(benzo[d][1,3]dioxol-4-yl)-2-[(tert-butoxycarbonyl)amino]acetic acid synthesized in the similar manner as in Reference Example 28 in 8 ml of DMF, 3.86 g (27.9 mmol) of potassium carbonate and 1.3 ml (21 mmol) of methyl iodide were added in this order at room temperature, stirred at the same temperature as above for 1 hour, and then left standing overnight.

After the completion of the reaction, the reaction solution was poured to 100 ml of a saturated aqueous solution of sodium chloride, and water was added until insoluble matter was dissolved, followed by extraction with toluene twice. The obtained organic layer was dried over anhydrous sodium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: hexane:ethyl acetate=95:5 to 70:30 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 2.83 g of the title compound (yield: 69%) as a white solid.

Mass spectrum (EI, m/z): 309 [M]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 6.85-6.76 (m, 3H), 6.03-5.97 (m, 2H), 5.71-5.61 (m, 1H), 5.49-5.39 (m, 1H), 3.73 (s, 3H), 1.47-1.39 (m, 9H).

Reference Example 30 tert-Butyl [1-(benzo[d][1,3]dioxol-4-yl)-2-hydroxyethyl]carbamate

To a solution of 2.82 g (9.13 mmol) of methyl 2-(benzo[d][1,3]dioxol-4-yl)-2-[(tert-butoxycarbonyl)amino]acetate synthesized in the similar manner as in Reference Example 29 in 30 ml of dehydrated THF, 716 mg (32.9 mmol) of lithium borohydride was added under cooling in ice water and stirred at room temperature.

After the completion of the reaction, the reaction solution was poured to 150 ml of a saturated aqueous solution of ammonium chloride, followed by extraction with ethyl acetate. The obtained organic layer was dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. Diethyl ether and n-hexane were added to the concentration residue, and the formed solid was filtered, washed by sousing with diethyl ether, and then dried under reduced pressure to obtain 1.54 g of the title compound (yield: 60%) as a white solid.

Mass spectrum (CI, m/z): 282 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.13 (d, J=8.3 Hz, 1H), 6.84-6.75 (m, 3H), 6.02-5.96 (m, 2H), 4.82 (t, J=5.6 Hz, 1H), 4.74-4.64 (m, 1H), 3.54-3.40 (m, 2H), 1.37 (s, 9H).

Reference Example 31 2-Amino-2-(benzo[d][1,3]dioxol-4-yl)ethanol

To a solution of 1.04 g (3.69 mmol) of tert-butyl [1-(benzo[d][1,3]dioxol-4-yl)-2-hydroxyethyl]carbamate synthesized in the similar manner as in Reference Example 30 in 17 ml of dichloromethane, 1.3 ml (11 mmol) of 2,6-lutidine and 2.0 ml (11 mmol) of trimethylsilyl trifluoromethanesulfonate were added in this order under cooling in ice water and stirred at the same temperature as above for 3 hours.

After the completion of the reaction, 14 ml of a saturated aqueous solution of sodium bicarbonate and 14 ml of dichloromethane were added to the reaction solution. The pH was adjusted to 10 to 11 by further adding a 4 N aqueous sodium hydroxide solution, followed by separation into an aqueous layer and an organic layer. The aqueous layer was subjected to extraction with dichloromethane twice, all of the obtained organic layers were dried over anhydrous sodium carbonate and filtered, and then, the filtrate was concentrated under reduced pressure. 2.5 ml of methanol and 2.5 ml of triethylamine were added to the obtained residue and stirred at room temperature for 7 hours. 5 ml of methanol was further added, then applied to a microwave reaction apparatus, and reacted at 80° C. for 1 hour. After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain 0.696 g of the title compound (containing impurities) as a pale yellow solid.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 6.95-6.91 (m, 1H), 6.81-6.75 (m, 2H), 5.98 (d, J=0.9 Hz, 1H), 5.95 (d, J=0.9 Hz, 1H), 4.86-4.63 (m, 1H), 3.96 (dd, J=4.4, 7.9 Hz, 1H), 3.51 (dd, J=4.4, 10.2 Hz, 1H), 3.40-3.21 (m, 1H), 1.98-1.72 (m, 2H).

Reference Example 32 1-(Benzo[d][1,3]dioxol-4-yl)-2-[(tert-butyldimethylsilyl)oxy]ethanamine

To a solution of 0.691 g of 2-amino-2-(benzo[d][1,3]dioxol-4-yl)ethanol (containing impurities) synthesized in the similar manner as in Reference Example 31 by using 1.04 g (3.69 mmol) of tert-butyl [1-(benzo[d][1,3]dioxol-4-yl)-2-hydroxyethyl]carbamate synthesized in the similar manner as in Reference Example 30, and 95.9 mg (0.785 mmol) of 4-(N,N-dimethylamino)pyridine in 7 ml of dichloromethane, 1.10 ml (7.89 mmol) of triethylamine and 580 mg (3.85 mmol) of chloro(tert-butyl)dimethylsilane were added and stirred at room temperature for 14 hours.

After the completion of the reaction, water and dichloromethane were added to the reaction solution, and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with dichloromethane twice, all of the obtained organic layers were dried over anhydrous sodium carbonate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (DNH silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. The obtained residue was subjected again to silica gel column chromatography (elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 0.810 g of the title compound (74% [2 steps]) as a pale yellow oil.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 6.95-6.91 (m, 1H), 6.81-6.76 (m, 2H), 5.97 (d, J=0.9 Hz, 1H), 5.95 (d, J=0.9 Hz, 1H), 3.99 (dd, J=5.5, 7.0 Hz, 1H), 3.64 (dd, J=5.5, 9.7 Hz, 1H), 3.53 (dd, J=7.0, 9.7 Hz, 1H), 1.81 (br s, 2H), 0.82 (s, 9H), −0.04 (s, 3H), −0.05 (s, 3H).

Reference Example 33 4-Amino-4-phenyl-2-butyn-1-ol hydrochloride

To a solution of 1.01 ml (7.28 mmol) of 2-(2-propynyloxy)tetrahydro-2H-pyran in 20 ml of dehydrated THF, 5.65 ml (7.35 mmol) of 1.3 mol/l lithium bis(trimethylsilyl)amide/THF solution was added with stirring at −78° C. in an argon atmosphere and stirred at the same temperature as above for 15 minutes. Subsequently, 1.02 g (4.87 mmol) of (E)-N-benzylidene-2-methylpropane-2-sulfinamide [synthesized according to the method described in Org. Lett., 2005, 7, 5493-5496] was added at −78° C., stirred at the same temperature as above for 1 hour, and then stirred for 1 hour after the temperature was raised to room temperature.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to obtain a concentration residue.

To a solution of 2.10 g of the obtained concentration residue in 20 ml of methanol, 4.85 ml (19.4 mmol) of 4 N hydrogen chloride/1,4-dioxane solution was added with stirring at 0° C. in an argon atmosphere and stirred for 3 hours after the temperature was raised to room temperature.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. For the obtained concentration residue, crystallization was performed with diisopropyl ether/methanol, and the deposited solid was collected by filtration, washed by sousing with diisopropyl ether, and then dried under reduced pressure to obtain 0.93 g of the title compound (yield: 97% [2 steps]) as a brown solid.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 8.97 (br s, 3H), 7.66-7.60 (m, 2H), 7.51-7.40 (m, 3H), 5.78-5.07 (m, 2H), 4.19 (d, J=1.8 Hz, 2H).

Reference Example 34 (S)-2-[(tert-Butoxycarbonyl)amino]-2-phenylethyl acetate

To 10 g (42 mmol) of (S)-tert-butyl(2-hydroxy-1-phenylethyl)carbamate [purchased from Novo Chemy Ltd.] and 7.1 ml (51 mmol) of triethylamine in 100 ml of dehydrated dichloromethane, 4.80 ml (50.8 mmol) of acetic anhydride was added dropwise at 0° C. in an argon atmosphere and stirred for 20 hours after the temperature was raised to room temperature.

After the completion of the reaction, 100 ml of a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with dichloromethane (100 ml) twice, and all of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=93:7 to 72:28 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 10.5 g of the title compound (yield: 89%) as a white solid.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.53 (d, J=8.9 Hz, 1H), 7.38-7.31 (m, 4H), 7.30-7.22 (m, 1H), 4.87-4.74 (m, 1H), 4.15 (dd, J=4.8, 11.0 Hz, 1H), 4.02 (dd, J=8.8, 11.0 Hz, 1H), 1.98 (s, 3H), 1.43-1.20 (m, 9H).

Reference Example 35 (S)-2-Amino-2-phenylethyl acetate hydrochloride

To a solution of 10.5 g (37.6 mmol) of (S)-2-[(tert-butoxycarbonyl)amino]-2-phenylethyl acetate synthesized in the similar manner as in Reference Example 34 in 110 ml of dehydrated dichloromethane, 47 ml (188 mmol) of 4 N hydrogen chloride/1,4-dioxane solution was added at room temperature in an argon atmosphere and stirred for 14 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. Diethyl ether was added to the obtained concentration residue, ultrasonicated, then filtered, and dried under reduced pressure to obtain 6.78 g of the title compound (yield: 84%) as a white solid.

Mass spectrum (DUIS, m/z): 180 [M (Free form)+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 8.80 (br s, 3H), 7.59-7.52 (m, 2H), 7.49-7.38 (m, 3H), 4.58 (dd, J=6.1, 6.1 Hz, 1H), 4.39-4.29 (m, 2H), 2.06 (s, 3H).

Reference Example 36 (S)-tert-Butyl [2-(benzyloxy)-1-phenylethyl]carbamate

To a solution of 10.01 g (42.2 mmol) of (S)-tert-butyl (2-hydroxy-1-phenylethyl)carbamate [purchased from Novo Chemy Ltd.] in 200 ml of dehydrated DMF, 2.58 g (64.5 mmol) of 60% sodium hydride was added at 0° C. in an argon atmosphere and stirred at the same temperature as above for 20 minutes. Subsequently, 5.50 ml (46.3 mmol) of benzyl bromide was added at 0° C. and stirred at the same temperature as above for 1 hour.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with water three times, and a saturated aqueous solution of sodium chloride once, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=95:5 to 80:20 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 9.94 g of the title compound (yield: 72%) as a white solid.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.44 (d, J=8.7 Hz, 1H), 7.37-7.21 (m, 10H), 4.84-4.73 (m, 1H), 4.49 (s, 2H), 3.61-3.46 (m, 2H), 1.46-1.15 (m, 9H).

Reference Example 37 (S)-Ethyl 5-{[2-(benzyloxy)-1-phenylethyl]carbamoyl}-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate

To a solution of 9.94 g (30.4 mmol) of (S)-tert-butyl [2-(benzyloxy)-1-phenylethyl]carbamate synthesized in the similar manner as in Reference Example 36 in 120 ml of dichloromethane, 30 ml of trifluoroacetic acid was added at room temperature in an argon atmosphere and stirred at the same temperature as above for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure and dried under reduced pressure to obtain 10.25 g of a concentration residue.

To a solution of 3.02 g of a portion of the obtained concentration residue and 3.10 ml (17.8 mmol) of DIPEA in 50 ml of dehydrated 1,4-dioxane, 1.95 g (4.42 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 was added at room temperature in an argon atmosphere and stirred at 60° C. for 8 hours.

After the completion of the reaction, water was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The obtained organic layer was washed with water and a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 1.86 g of the title compound (yield: 67%) as a white foam.

Mass spectrum (DUIS, m/z): 632 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.80 (s, 1H), 7.43-7.18 (m, 10H), 6.56 (d, J=8.2 Hz, 1H), 5.11-5.03 (m, 1H), 4.66 (d, J=13.8 Hz, 1H), 4.60 (d, J=13.8 Hz, 1H), 4.52 (s, 2H), 4.42 (q, J=7.1 Hz, 2H), 3.74 (dd, J=8.0, 10.0 Hz, 1H), 3.63 (dd, J=6.0, 10.0 Hz, 1H), 2.58-2.52 (m, 2H), 2.31-2.22 (m, 2H), 1.95-1.84 (m, 2H), 1.62 (s, 3H), 1.55 (s, 3H), 1.34 (t, J=7.1 Hz, 3H), 0.12 (s, 9H).

Reference Example 38 (S)-Ethyl 5-[(2-hydroxy-1-phenylethyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate

To a solution of 1.86 g (2.94 mmol) of (S)-ethyl 5-{([2-(benzyloxy)-1-phenylethyl]carbamoyl}-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 37 in 30 ml of 2-propanol, 0.19 g of 20% palladium hydroxide/carbon (containing 50 wt % water) was added at room temperature in an argon atmosphere and then, after replacement with a hydrogen atmosphere under reduced pressure, stirred at room temperature for 1.5 hours. After replacement with an argon atmosphere, the reaction solution was filtered through celite. The solid on the celite was washed with ethyl acetate, and then, the filtrate was concentrated under reduced pressure. To a solution of the obtained concentration residue in 30 ml of 2-propanol, 0.19 g of 20% palladium hydroxide/carbon (containing 50 wt % water) was added at room temperature in an argon atmosphere and after replacement with a hydrogen atmosphere under reduced pressure, stirred at room temperature for 3.5 hours.

After the completion of the reaction, replacement with an argon atmosphere was performed, and then, the reaction solution was filtered through celite. The solid on the celite was washed with ethyl acetate, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=80:20 to 60:40 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 1.34 g of the title compound (yield: 84%) as a white foam.

Mass spectrum (DUIS, m/z): 542 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.81 (s, 1H), 7.38-7.26 (m, 4H), 7.23-7.17 (m, 1H), 6.36 (d, J=7.5 Hz, 1H), 4.87 (t, J=6.0 Hz, 1H), 4.82-4.75 (m, 1H), 4.66 (s, 2H), 4.42 (q, J=7.2 Hz, 2H), 3.67-3.55 (m, 2H), 2.60-2.52 (m, 2H), 2.31-2.21 (m, 2H), 1.96-1.85 (m, 2H), 1.62 (s, 3H), 1.54 (s, 3H), 1.34 (t, J=7.2 Hz, 3H), 0.13 (s, 9H).

Reference Example 39 (S)-Benzyl {2-[(tert-butoxycarbonyl)amino]-2-phenylethyl} succinate

To a solution of 496 mg (2.09 mmol) of (S)-tert-butyl (2-hydroxy-1-phenylethyl)carbamate [purchased from Novo Chemy Ltd.] and 227 mg (2.26 mmmol) of succinic anhydride in 3 ml of dehydrated DMF, 26.2 mg (0.214 mmol) of 4-dimethylaminopyridine was added at room temperature in a nitrogen atmosphere and stirred at room temperature for 3 hours. Subsequently, 0.270 ml (2.27 mmol) of benzyl bromide was added at room temperature and stirred at room temperature for 15 hours.

After the completion of the reaction, toluene was added to the reaction solution, the organic layer obtained after washing with water twice and a saturated aqueous solution of sodium chloride once was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=86:14 to 65:35 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 872 mg of the title compound (yield: 98%) as a white solid.

Mass spectrum (CI, m/z): 428 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.39-7.25 (m, 10H), 5.21-5.08 (m, 3H), 5.04-4.90 (m, 1H), 4.39-4.21 (m, 2H), 2.70-2.59 (m, 4H), 1.42 (br s, 9H).

Reference Example 40 (S)-2-Amino-2-phenylethyl benzyl succinate trifluoroacetate

To a solution of 608 mg (1.42 mmol) of (S)-benzyl {2-[(tert-butoxycarbonyl)amino]-2-phenylethyl} succinate synthesized in the similar manner as in Reference Example 39 in 10 ml of dichloromethane, 2.0 ml (26 mmol) of trifluoroacetic acid was added at room temperature in a nitrogen atmosphere and stirred at room temperature for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and the operation of adding toluene to the obtained concentration residue and concentrating the resultant under reduced pressure was repeated several times to obtain 813 mg of the title compound (containing impurities).

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 8.57 (br s, 3H), 7.53-7.30 (m, 10H), 5.09 (s, 2H), 4.67-4.55 (m, 1H), 4.38-4.27 (m, 2H), 2.66 (s, 4H).

Reference Example 41 (S)-{2-[(tert-Butoxycarbonyl)amino]-2-phenylethoxy}methyl pivalate

To a solution of 4.09 g (17.2 mmol) of (S)-tert-butyl (2-hydroxy-1-phenylethyl)carbamate [purchased from Novo Chemy Ltd.] in 80 ml of dehydrated THF, 0.762 g (19.1 mmol) of 60 wt % sodium hydride was added at 0° C. in a nitrogen atmosphere and stirred at the same temperature as above for 1 hour. Subsequently, 2.65 ml (18.3 mmol) of chloromethyl pivalate was added at 0° C. and stirred at the same temperature as above for 25 minutes and further for 2.5 hours after the temperature was raised to room temperature.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution and stirred, followed by extraction with a mixed solvent of ethyl acetate and n-hexane twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=95:5 to 75:25 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 3.32 g of the title compound (yield: 55%) as a white solid.

Mass spectrum (CI, m/z): 352 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.36-7.23 (m, 5H), 5.27 (d, J=6.3 Hz, 1H), 5.33-5.21 (m, 1H), 5.19 (d, J=6.3 Hz, 1H), 4.80 (br s, 1H), 3.91 (dd, J=4.4, 9.6 Hz, 1H), 3.87-3.77 (m, 1H), 1.41 (br s, 9H), 1.18 (s, 9H).

Reference Example 42 (S)-(2-Amino-2-phenylethoxy)methyl pivalate

To a solution of 3.32 g (9.45 mmol) of (S)-{2-[(tert-butoxycarbonyl)amino]-2-phenylethoxy}methyl pivalate synthesized in the similar manner as in Reference Example 41 in 50 ml of dehydrated dichloromethane, 6.0 ml (78 mmol) of trifluoroacetic acid was added at 0° C. in a nitrogen atmosphere, stirred at the same temperature as above for 2 hours, and then stirred for 70 minutes after the temperature was raised to room temperature.

After the completion of the reaction, the reaction solution was poured to a saturated aqueous solution of sodium bicarbonate for neutralization, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DNH silica gel, elution solvent: n-hexane:ethyl acetate=95:5 to 80:20 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 1.83 g of the title compound (yield: 77%) as a colorless oil.

Mass spectrum (CI, m/z): 252 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.40-7.24 (m, 5H), 5.36 (d, J=6.1 Hz, 1H), 5.26 (d, J=6.1 Hz, 1H), 4.21 (dd, J=3.8, 8.8 Hz, 1H), 3.78 (dd, J=3.8, 9.6 Hz, 1H), 3.59 (dd, J=8.8, 9.6 Hz, 1H), 1.21 (s, 9H).

Reference Example 43 (S)-2-({[(2,5-Dioxopyrrolidin-1-yl)oxy]carbonyl}oxy)-2-phenylethyl acetate

To a solution of 0.84 g (4.7 mmol) of (S)-2-hydroxy-2-phenylethyl acetate [synthesized according to the method described in J. Org. Chem., 2013, 78 (22), 11618-11622] in 30 ml of dehydrated acetonitrile, 0.90 ml (6.4 mmol) of triethylamine and 1.33 g (5.19 mmol) of N,N′-disuccinimidyl carbonate were added in this order at room temperature in a nitrogen atmosphere and stirred at the same temperature as above for 15 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The obtained concentration residue was dissolved in ethyl acetate, and it was washed with water. An organic layer and an aqueous layer were separated, and then, the aqueous layer was subjected to extraction with ethyl acetate once. All of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=85:15 to 60:40 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 1.28 g of the title compound (yield: 85%) as a colorless oil.

Mass spectrum (CI, m/z): 322 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.45-7.34 (m, 5H), 5.95 (dd, J=5.2, 7.2 Hz, 1H), 4.39 (d, J=5.2 Hz, 1H), 4.38 (d, J=7.2 Hz, 1H), 2.83 (s, 4H), 2.12 (s, 3H).

Reference Example 44 (S)-Benzyl 2-[(tert-butoxycarbonyl)amino]-2-phenylacetate

To a solution of 2.50 g (9.95 mmol) of (S)-2-[(tert-butoxycarbonyl)amino]-2-phenylacetic acid in 30 ml of DMF, 1.47 g (10.6 mmol) of potassium carbonate was dividedly added with stirring at room temperature in a nitrogen atmosphere, and subsequently, 1.20 ml (10.1 mmol) of benzyl bromide was added dropwise at room temperature, stirred at the same temperature as above for 7 hours, and then left at room temperature for 3 days.

After the completion of the reaction, toluene was added to the reaction solution and washed with water twice. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and then concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 79:21 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 3.24 g of the title compound (yield: 95%) as a white solid.

Mass spectrum (CI, m/z): 342 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.37-7.27 (m, 8H), 7.23-7.15 (m, 2H), 5.61-5.50 (m, 1H), 5.40-5.33 (m, 1H), 5.23-5.08 (m, 2H), 1.49-1.29 (m, 9H).

Reference Example 45 (S)-Benzyl 2-amino-2-phenylacetate trifluoroacetate

To a solution of 462 mg (1.35 mmol) of (S)-benzyl 2-[(tert-butoxycarbonyl)amino]-2-phenylacetate synthesized in the similar manner as in Reference Example 44 in 10 ml of dichloromethane, 2.0 ml (26 mmol) of trifluoroacetic acid was added at room temperature and stirred at room temperature for 24 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The operation of adding dichloromethane to the obtained concentration residue and concentrating the resultant under reduced pressure was repeated several times to obtain 572 mg of the title compound (containing impurities).

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 8.93 (br s, 3H), 7.54-7.44 (m, 5H), 7.38-7.31 (m, 3H), 7.27-7.21 (m, 2H), 5.40 (br s, 1H), 5.27 (d, J=12.5 Hz, 1H), 5.21 (d, J=12.5 Hz, 1H).

Reference Example 46 Ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate

To a solution of 9.70 g (61.3 mmol) of 1-(trimethylsilyl)cyclopropanecarboxylic acid [synthesized according to the method described in J. Org. Chem., 1982 (47) 5, 893-895] in 120 ml of dehydrated dichloromethane, 6.60 ml (76.9 mmol) of oxalyl chloride and 0.25 ml (3.2 mmol) of dehydrated DMF were added in this order at 0° C. in a nitrogen atmosphere and then stirred for 2.5 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure and dried under reduced pressure to obtain a concentration residue.

To a solution of 19.0 ml (109 mmol) of DIPEA and 9.94 g (30.6 mmol) of 5-tert-butyl 2-ethyl 3-amino-6,6-dimethylpyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate [synthesized according to the method described in Journal of Medicinal Chemistry 2012, 55 (10), 4728-4739] in 170 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 30 ml of dehydrated dichloromethane was added at 0° C. in a nitrogen atmosphere and then stirred for 24 hours with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred, followed by extraction with dichloromethane once and ethyl acetate twice. All of the obtained organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 70:30 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. A concentration residue of a fraction containing impurities was subjected again to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 75:25 (V/V)), combined with the purified form obtained above, concentrated under reduced pressure, and dried under reduced pressure to obtain 10.63 g of a concentration residue.

To a solution of the obtained concentration residue in 100 ml of ethyl acetate, 60.0 ml (240 mmol) of 4 N hydrogen chloride/ethyl acetate was added at room temperature in a nitrogen atmosphere and then stirred for 5 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. The obtained concentration residue was suspended in diisopropyl ether, and the suspension was stirred at room temperature. Insoluble matter was collected by filtration, and the obtained solid was washed with diisopropyl ether. The obtained solid was dissolved in water, and then, a saturated aqueous solution of sodium bicarbonate and dichloromethane were added and stirred at room temperature for 5 minutes. After separation into an aqueous layer and an organic layer, the aqueous layer was subjected to extraction with dichloromethane twice. All of the organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and dried under reduced pressure to obtain 8.27 g of the title compound (yield: 73% [2 steps]) as a light orange solid.

Mass spectrum (DUIS, m/z): 365 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 10.02 (s, 1H), 4.53 (q, J=7.2 Hz, 2H), 4.16 (s, 2H), 1.50-1.43 (m, 9H), 1.14-1.08 (m, 2H), 0.84-0.77 (m, 2H), 0.12 (s, 9H).

Reference Example 47 N-(2,2-Difluoro-3-hydroxy-1-phenylpropyl)-2-methylpropane-2-sulfinamide

To 32 ml of degassed dehydrated THF, 3.29 g (50.3 mmol) of an active zinc powder was added at room temperature in an argon atmosphere and then heated to 40° C. Subsequently, 8.60 ml (66.1 mmol) of ethyl bromodifluoroacetate was dividedly added to the reaction solution at 40° C. and then stirred at 40° C. for 1 hour. To the reaction solution allowed to cool to room temperature, a solution of 3.47 g (16.6 mmol) of N-benzylidene-2-methylpropane-2-sulfinamide [synthesized according to the method described in Org. Lett., 2005, 7, 5493-5496] in 18 ml of dehydrated THF was added at room temperature and then stirred at room temperature for 23 hours.

After the completion of the reaction, ethyl acetate and a saturated aqueous solution of sodium bicarbonate were added to the reaction solution and then stirred at room temperature for 10 minutes. The obtained suspension was filtered using a celite filter, subsequently the removed solid was washed with ethyl acetate, and then, the filtrate was separated into an aqueous layer and an organic layer. The aqueous layer was subjected to extraction with ethyl acetate twice, and then, all of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=85:15 to 65:35 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 4.08 g of a concentration residue.

To a solution of 1.01 g of a portion of the obtained concentration residue in 20 ml of dehydrated THF, 136 mg (6.23 mmol) of lithium borohydride was added at room temperature in a nitrogen atmosphere and then stirred for 1.5 hours with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added dropwise to the reaction solution until foaming settled, and then, an excessive amount of a saturated aqueous solution of ammonium chloride was further added and stirred at room temperature for 10 minutes. Subsequently, extraction was performed with ethyl acetate three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=80:20 to 50:50 (V/V)), subsequently concentrated under reduced pressure, and dried under reduced pressure to obtain 573 mg of the title compound (yield: 48% [2 steps]) as a colorless oil.

Mass spectrum (CI, m/z): 292 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.42-7.33 (m, 5H), 4.97-4.85 (m, 1H), 4.37 (d, J=6.8 Hz, 1H), 4.03-3.74 (m, 3H), 1.25 (s, 9H).

Reference Example 48 3-Amino-2,2-difluoro-3-phenylpropan-1-ol

To a solution of 568 mg (1.95 mmol) of N-(2,2-difluoro-3-hydroxy-1-phenylpropyl)-2-methylpropane-2-sulfinamide synthesized in the similar manner as in Reference Example 47 in 5 ml of ethanol, 2.0 ml (8.0 mmol) of 4 N hydrogen chloride/1,4-dioxane was added at room temperature in a nitrogen atmosphere and then stirred for 1.5 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was neutralized by adding a saturated aqueous solution of sodium bicarbonate, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=70:30 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 254 mg of the title compound (yield: 70%) as a white solid.

Mass spectrum (CI, m/z): 188 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.46-7.32 (m, 5H), 4.44 (dd, J=9.8, 13.1 Hz, 1H), 3.88 (ddd, J=8.6, 12.4, 17.8 Hz, 1H), 3.79-3.67 (m, 1H).

Reference Example 49 2-(2-Isopropoxy-1-phenylethyl)isoindolin-1,3-dione

To a solution of 0.500 g (2.78 mmol) of 2-isopropoxy-1-phenylethanol [synthesized according to the method described in J. Fluorine Chem., 2004, 125, 1779-1790], 0.818 g (5.56 mmol) of isoindolin-1,3-dione, and 1.46 g (5.57 mmol) of triphenylphosphine in 20 ml of dehydrated dichloromethane, 1.10 ml (5.66 mmol) of diisopropyl azodicarboxylate was added with stirring at 0° C. in an argon atmosphere, then brought back to room temperature, and stirred at room temperature for 16 hours.

A 5% aqueous potassium bisulfate solution was added to the reaction solution and separated into an aqueous layer and an organic layer. The organic layer was washed with a saturated aqueous solution of sodium bicarbonate, dried over anhydrous magnesium sulfate, and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=93:7 to 72:28 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 0.677 g of the title compound (yield: 79%) as a colorless oil.

Mass spectrum (CI, m/z): 310 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.93-7.83 (m, 4H), 7.47-7.41 (m, 2H), 7.39-7.27 (m, 3H), 5.44 (dd, J=6.0, 9.9 Hz, 1H), 4.33 (t, J=9.9 Hz, 1H), 4.01 (dd, J=6.0, 9.9 Hz, 1H), 3.61 (spt, J=6.1 Hz, 1H), 1.02 (d, J=6.1 Hz, 3H), 0.98 (d, J=6.1 Hz, 3H).

Reference Example 50 2-Isopropoxy-1-phenylethanamine

To a solution of 0.670 g (2.17 mmol) of 2-(2-isopropoxy-1-phenylethyl)isoindolin-1,3-dione synthesized in the similar manner as in Reference Example 49 in 10 ml of ethanol, 0.37 ml (6.5 mmol) of acetic acid and 0.32 ml (6.6 mmol) of hydrazine monohydrate were added in an argon atmosphere and heated to reflux for 3 hours.

After standing to cool, ethanol was added and filtered, and the filtrate was concentrated under reduced pressure. Dichloromethane and a 5% aqueous sodium carbonate solution were added to the residue and stirred at room temperature. After separation into an aqueous layer and an organic layer, the organic layer was dried over anhydrous sodium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 0.348 g of the title compound (yield: 90%) as a colorless oil.

Mass spectrum (CI, m/z): 180 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.43-7.37 (m, 2H), 7.37-7.30 (m, 2H), 7.29-7.23 (m, 1H), 4.17 (dd, J=3.6, 9.2 Hz, 1H), 3.66-3.55 (m, 2H), 3.31 (t, J=9.2 Hz, 1H), 1.20-1.14 (m, 6H).

Reference Example 51 2-(2-Phenoxy-1-phenylethyl)isoindolin-1,3-dione

To a solution of 1.04 g (4.85 mmol) of 2-phenoxy-1-phenylethanol [synthesized according to the method described in J. Org. Chem., 2011, 76, 1883-1886], 1.40 g (9.52 mmol) of isoindolin-1,3-dione, and 2.45 g (9.34 mmol) of triphenylphosphine in 40 ml of dehydrated dichloromethane, 1.90 ml (9.77 mmol) of diisopropyl azodicarboxylate was added with stirring at 0° C. in an argon atmosphere, then brought back to room temperature, and stirred at room temperature for 20 hours.

A 5% aqueous potassium bisulfate solution was added to the reaction solution and separated into an aqueous layer and an organic layer. The organic layer was washed with a saturated aqueous solution of sodium bicarbonate, dried over anhydrous magnesium sulfate, and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=93:7 to 72:28 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 1.15 g of the title compound (containing impurities) as a colorless viscous liquid.

Mass spectrum (CI, m/z): 344[M+1]⁺.

Reference Example 52 2-Phenoxy-1-phenylethanamine

To a solution of 1.14 g of 2-(2-phenoxy-1-phenylethyl)isoindolin-1,3-dione (containing impurities) synthesized in Reference Example 51 in 15 ml of ethanol, 0.60 ml (10 mmol) of acetic acid was added with stirring in a nitrogen atmosphere, and subsequently, 0.50 ml (10 mmol) of hydrazine monohydrate was added at room temperature and then heated to reflux for 2.5 hours.

After standing to cool, ethanol was added and filtered, and the filtrate was concentrated under reduced pressure. 50 ml of dichloromethane and 50 ml of a 5% aqueous sodium carbonate solution were added to the residue and stirred at room temperature. After separation into an aqueous layer and an organic layer, the organic layer was dried over anhydrous sodium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:methanol=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 0.59 g of the title compound (yield: 58% [2 steps]) as a colorless oil.

Mass spectrum (CI, m/z): 214 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.49-7.43 (m, 2H), 7.41-7.24 (m, 5H), 6.98-6.88 (m, 3H), 4.43 (dd, J=3.7, 9.0 Hz, 1H), 4.09 (dd, J=3.7, 9.0 Hz, 1H), 3.92 (t, J=9.0 Hz, 1H).

Reference Example 53 3,3,8,8,9,9-Hexamethyl-5-phenyl-2,4,7-trioxa-8-siladecane

A solution of 1.78 g (7.05 mmol) of 2-[(tert-butyldimethylsilyl)oxy]-1-phenylethanol [synthesized according to the method described in WO 2011/19090, page 43] in 35 ml of dehydrated dichloromethane was cooled in ice, and 0.86 ml (9.1 mmol) of 2-methoxy-1-propene and subsequently 0.180 g (0.716 mmol) of pyridinium p-toluenesulfonate were added thereto in a nitrogen atmosphere and stirred at the same temperature as above for 3 hours.

20 ml of a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, stirred, and then separated into an aqueous layer and an organic layer. The aqueous layer was subjected to extraction with dichloromethane, all of the obtained organic layers were dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=99:1 to 94:6 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 1.38 g of the title compound (yield: 60%) as a colorless oil.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.39-7.18 (m, 5H), 4.74 (dd, J=5.4, 7.3 Hz, 1H), 3.75 (dd, J=7.3, 10.4 Hz, 1H), 3.54 (dd, J=5.4, 10.4 Hz, 1H), 3.15 (s, 3H), 1.42 (s, 3H), 1.12 (s, 3H), 0.84 (s, 9H), −0.04 (s, 3H), −0.07 (s, 3H).

Reference Example 54 2-[(2-Methoxypropan-2-yl)oxy]-2-phenylethanol

To a solution of 1.36 g (4.19 mmol) of 3,3,8,8,9,9-hexamethyl-5-phenyl-2,4,7-trioxa-8-siladecane synthesized in the similar manner as in Reference Example 53 in 24 ml of dehydrated THF, 6.3 ml (6.3 mmol) of 1 M tetra-n-butylammonium fluoride/THF solution was added dropwise with stirring at 0° C. in a nitrogen atmosphere and stirred at the same temperature as above for 2 hours.

A saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with a n-hexane/ethyl acetate mixed solution (1:1 (V/V)) three times. The extracts were dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=84:16 to 63:37 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 0.697 g of the title compound (yield: 79%) as a colorless oil.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.37-7.23 (m, 5H), 4.84 (dd, J=4.8, 7.0 Hz, 1H), 3.70-3.58 (m, 2H), 3.18 (s, 3H), 2.34-2.20 (m, 1H), 1.44 (s, 3H), 1.21 (s, 3H).

Reference Example 55 2,5-Dioxopyrrolidin-1-yl {2-[(2-methoxypropan-2-yl)oxy]-2-phenylethyl}carbonate

To a solution of 0.685 g (3.26 mmol) of 2-[(2-methoxypropan-2-yl)oxy]-2-phenylethanol synthesized in the similar manner as in Reference Example 54 in 20 ml of dehydrated acetonitrile, 1.00 g (3.90 mmol) of bis(2,5-dioxopyrrolidin-1-yl)carbonate and 0.70 ml (5.0 mmol) of triethylamine were added with stirring at room temperature in a nitrogen atmosphere and stirred at room temperature for 3 hours.

The reaction solution was concentrated under reduced pressure, and water was added to the residue, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=71:29 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 0.636 g of the title compound (yield: 56%) as a colorless viscous liquid.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.42-7.27 (m, 5H), 5.04 (dd, J=3.7, 8.8 Hz, 1H), 4.41 (dd, J=8.8, 11.1 Hz, 1H), 4.24 (dd, J=3.7, 11.1 Hz, 1H), 3.17 (s, 3H), 2.83 (s, 4H), 1.45 (s, 3H), 1.13 (s, 3H).

Reference Example 56 2-[(2-Methoxypropan-2-yl)oxy]-2-phenylethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-4,6-dihydropyrrolo[3,4-c]pyrazole-5-(1H)-carboxylate

To a solution of 0.102 g (0.269 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate synthesized in the similar manner as in Reference Example 5 and 0.145 g (0.411 mmol) of 2,5-dioxopyrrolidin-1-yl {2-[(2-methoxypropan-2-yl)oxy]-2-phenylethyl}carbonate synthesized in the similar manner as in Reference Example 55 in 3 ml of dehydrated dichloromethane, 0.14 ml (0.80 mmol) of DIPEA was added at room temperature in a nitrogen atmosphere and stirred at room temperature for 1.5 hours. The reaction solution was concentrated under reduced pressure, and 2.5 ml of methanol and 0.080 ml (1.3 mmol) of 2-aminoethanol were added at room temperature and stirred at room temperature for 14 hours.

The reaction solution was concentrated under reduced pressure, water was added, the organic layer after extraction with ethyl acetate was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:ethyl acetate=100:0 to 84:16 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 0.127 g of the title compound (containing impurities) as a white foam.

Mass spectrum (DUIS, m/z): 541 [M−1]⁻.

Reference Example 57 Ethyl 6,6-dimethyl-5-(2-phenoxyacetyl)-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate

To a solution of 0.180 g (1.19 mmol) of 2-phenoxyacetic acid in 3 ml of dehydrated dichloromethane, 0.005 ml (0.07 mmol) of DMF was added at room temperature in a nitrogen atmosphere and then cooled in ice. Subsequently, 0.102 ml (1.19 mmol) of oxalyl chloride was added dropwise at 0° C. and after the completion of the dropwise addition, stirred at room temperature for 2 hours. Then, the reaction solution was concentrated under reduced pressure at room temperature.

To a solution of 0.171 g (0.388 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 in 3.5 ml of dehydrated dichloromethane, 0.35 ml (2.0 mmol) of DIPEA was added at room temperature in a nitrogen atmosphere, and subsequently, a solution of the concentration residue obtained by the operation described above in 3 ml of dehydrated dichloromethane was added with stirring at 0° C. and then stirred at room temperature for 2 hours. Subsequently, 5 ml of 2-propanol was added and stirred at room temperature for 18 hours.

The reaction solution was concentrated under reduced pressure, the residue was subjected to silica gel column chromatography (elution solvent: 1,2-dichloroethane:ethyl acetate=100:0 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 0.148 g of the title compound (yield: 74%) as a pale yellow foam.

Mass spectrum (DUIS, m/z): 513 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.78 (s, 1H), 7.30-7.24 (m, 2H), 6.99-6.90 (m, 3H), 4.89-4.75 (m, 4H), 4.43 (q, J=7.1 Hz, 2H), 2.56-2.44 (m, 2H), 2.32-2.20 (m, 2H), 1.96-1.83 (m, 2H), 1.66 (s, 6H), 1.35 (t, J=7.1 Hz, 3H), 0.12 (s, 9H).

Reference Example 58 Ethyl 3-(benzyloxy)-2-bromopropanoate

To a solution of 2.00 g (7.72 mmol) of 3-(benzyloxy)-2-bromopropanoic acid [synthesized according to the method described in WO 2008/128942, page 38] in 20 ml of ethanol, 1.00 ml (18.8 mmol) of concentrated sulfuric acid was added with stirring at room temperature in an argon atmosphere and stirred at 80° C. for 5 hours.

After the completion of the reaction, the reaction solution allowed to cool to room temperature was concentrated under reduced pressure. The obtained concentration residue was neutralized by adding a 1 N aqueous sodium hydroxide solution, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure to obtain 2.00 g of the title compound (containing impurities) as a colorless oil.

Mass spectrum (CI, m/z): 287, 289 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.38-7.27 (m, 5H), 4.59 (s, 2H), 4.32 (dd, J=5.9, 8.4 Hz, 1H), 4.29-4.21 (m, 2H), 3.97 (dd, J=8.4, 10.2 Hz, 1H), 3.79 (dd, J=5.9, 10.2 Hz, 1H), 1.30 (t, J=7.2 Hz, 3H).

Reference Example 59 Ethyl 3-(benzyloxy)-2-phenoxypropanoate

To a solution of 1.31 g (13.9 mmol) of phenol in 20 ml of dehydrated DMF, 608 mg (13.9 mmol) of 55% sodium hydride was dividedly added with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 30 minutes. Subsequently, a solution of 2.00 g of ethyl 3-(benzyloxy)-2-bromopropanoate (containing impurities) synthesized in the similar manner as in Reference Example 58 in 5 ml of dehydrated DMF was added dropwise at 0° C. and then stirred at room temperature for 1 hour.

After the completion of the reaction, ice water was added to the reaction solution and neutralized with 1 N hydrochloric acid, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 80:20 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 1.10 g of the title compound (yield: 53%) as a colorless oil.

Mass spectrum (CI, m/z): 301 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.42-7.21 (m, 7H), 7.02-6.89 (m, 3H), 4.91-4.78 (m, 1H), 4.68 (d, J=12.2 Hz, 1H), 4.64 (d, J=12.2 Hz, 1H), 4.23 (q, J=7.1 Hz, 2H), 3.99-3.91 (m, 2H), 1.24 (t, J=7.1 Hz, 3H).

Reference Example 60 3-(Benzyloxy)-2-phenoxypropanoic acid

To a solution of 400 mg (1.33 mmol) of ethyl 3-(benzyloxy)-2-phenoxypropanoate synthesized in the similar manner as in Reference Example 59 in 10 ml of THF, 12 ml (12 mmol) of a 1 N aqueous sodium hydroxide solution was added with stirring at room temperature and stirred at 80° C. for 3 hours.

After the completion of the reaction, 1 N hydrochloric acid was added to the reaction solution at 0° C. to adjust the pH to 2, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure to obtain 341 mg of the title compound (containing impurities) as a white solid.

Mass spectrum (CI, m/z): 273 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.42-7.21 (m, 7H), 7.08-6.90 (m, 3H), 4.91-4.85 (m, 1H), 4.67 (d, J=12.3 Hz, 1H), 4.63 (d, J=12.3 Hz, 1H), 4.03-3.90 (m, 2H).

Reference Example 61 Methyl 2-bromo-3-methoxypropanoate

To a solution prepared by adding 20 ml of dehydrated methanol to 2.50 g (13.0 mmol) of a solution of 28% sodium methoxide in methanol, a solution of 3.00 g (11.5 mmol) of ethyl 2,3-dibromopropanoate in 20 ml of dehydrated methanol was added dropwise with stirring at 0° C. in an argon atmosphere and then stirred at room temperature for 2 hours.

After the completion of the reaction, 1 N hydrochloric acid was added thereto for neutralization and then concentrated under reduced pressure. The operation of adding toluene to the obtained concentration residue and concentrating the resultant under reduced pressure was repeated several times. Toluene was added, precipitates were filtered off, and the filtrate was concentrated under reduced pressure and dried under reduced pressure to obtain 580 mg of the title compound (yield: 26%) as an orange oil.

Mass spectrum (CI, m/z): 197 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 4.33 (dd, J=5.8, 8.2 Hz, 1H), 3.90 (dd, J=8.2, 10.2 Hz, 1H), 3.81 (s, 3H), 3.72 (dd, J=5.8, 10.2 Hz, 1H), 3.41 (s, 3H).

Reference Example 62 Methyl 3-methoxy-2-phenoxypropanoate

To a solution of 555 mg (5.90 mmol) of phenol in 10 ml of dehydrated DMF, 260 mg (5.96 mmol) of 55% sodium hydride was dividedly added with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 30 minutes. Subsequently, a solution of 580 mg (2.94 mmol) of methyl 2-bromo-3-methoxypropanoate synthesized in the similar manner as in Reference Example 61 in 10 ml of dehydrated DMF was added dropwise at 0° C. and then stirred at room temperature for 16 hours.

After the completion of the reaction, ice water was added to the reaction solution and then neutralized by adding 1 N hydrochloric acid, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 80:20 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 380 mg of the title compound (yield: 61%) as a colorless oil.

Mass spectrum (CI, m/z): 211 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.33-7.23 (m, 2H), 7.03-6.96 (m, 1H), 6.95-6.88 (m, 2H), 4.84 (dd, J=3.8, 5.3 Hz, 1H), 3.91 (dd, J=5.3, 10.5 Hz, 1H), 3.86 (dd, J=3.8, 10.5 Hz, 1H), 3.78 (s, 3H), 3.46 (s, 3H).

Reference Example 63 3-Methoxy-2-phenoxypropanoic acid

To a solution of 120 mg (0.571 mmol) of methyl 3-methoxy-2-phenoxypropanoate synthesized in the similar manner as in Reference Example 62 in 2 ml of THF, 0.700 ml (0.700 mmol) of a 1 N aqueous sodium hydroxide solution was added with stirring at room temperature and stirred at the same temperature as above for 3 hours.

After the completion of the reaction, the reaction solution was adjusted to pH 2 by adding 1 N hydrochloric acid, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure to obtain 116 mg of the title compound (containing impurities) as a brown solid.

Mass spectrum (CI, m/z): 197 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.34-7.25 (m, 2H), 7.06-7.00 (m, 1H), 6.99-6.91 (m, 2H), 4.90-4.81 (m, 1H), 3.98-3.84 (m, 2H), 3.46 (s, 3H).

Reference Example 64 Ethyl 3-hydroxy-2-phenoxypropanoate

To a solution of 3.00 g (9.99 mmol) of ethyl 3-(benzyloxy)-2-phenoxypropanoate synthesized in the similar manner as in Reference Example 59 in 20 ml of ethanol, 200 mg of 20% palladium hydroxide/carbon (containing 50% water) was added in an argon atmosphere and after replacement with a hydrogen atmosphere, stirred at room temperature for 2 hours.

After the completion of the reaction, replacement with an argon atmosphere was performed, and the reaction solution was filtered through celite. The solid on the celite was washed with ethanol, and all of the filtrates were concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=80:20 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 1.89 g of the title compound (yield: 90%) as a colorless oil.

Mass spectrum (CI, m/z): 211 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.35-7.25 (m, 2H), 7.05-6.97 (m, 1H), 6.95-6.88 (m, 2H), 4.78 (dd, J=3.8, 5.3 Hz, 1H), 4.29-4.22 (m, 2H), 4.15-4.01 (m, 2H), 2.22 (t, J=7.0 Hz, 1H), 1.26 (t, J=7.1 Hz, 3H).

Reference Example 65 Ethyl 3-(dimethylamino)-2-phenoxypropanoate

To a solution of 470 mg (2.24 mmol) of ethyl 3-hydroxy-2-phenoxypropanoate synthesized in the similar manner as in Reference Example 64 in 12 ml of dehydrated dichloromethane, 1.10 g (2.59 mmol) of Dess-Martin periodinane was added at 0° C. in an argon atmosphere and stirred at room temperature for 1 hour.

After the completion of the reaction, an aqueous sodium thiosulfate solution and a saturated aqueous solution of sodium bicarbonate were added to the reaction solution and stirred for 30 minutes, followed by extraction with dichloromethane. The organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and then, the filtrate was concentrated under reduced pressure.

To a solution of 470 mg of the obtained concentration residue in 6 ml of dehydrated dichloromethane, 0.260 ml (4.54 mmol) of acetic acid and 4.50 ml (9.00 mmol) of a solution of dimethylamine in THF were added in this order with stirring at room temperature in an argon atmosphere and then stirred at room temperature for 30 minutes. Subsequently, 720 mg (3.40 mmol) of sodium triacetoxyborohydride was dividedly added at 0° C. and stirred at room temperature for 16 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 80:20 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure.

To a solution of 162 mg of the obtained concentration residue in 4 ml of ethanol, 75 mg of 10% palladium/carbon (containing 54% water, PE-type manufactured by N.E. Chemcat Corp.) was added in an argon atmosphere and after replacement with a hydrogen atmosphere, stirred at room temperature for 3 hours.

After the completion of the reaction, replacement with an argon atmosphere was performed, and the reaction solution was filtered through celite. The solid on the celite was washed with ethanol, and all of the filtrates were concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=50:50 to 0:100 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 94 mg of the title compound (yield: 18% [3 steps]) as a colorless oil.

Mass spectrum (CI, m/z): 238 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.32-7.22 (m, 2H), 7.01-6.94 (m, 1H), 6.94-6.85 (m, 2H), 4.79 (dd, J=4.4, 7.2 Hz, 1H), 4.22 (q, J=7.1 Hz, 2H), 2.94 (dd, J=7.2, 13.2 Hz, 1H), 2.85 (dd, J=4.4, 13.2 Hz, 1H), 2.36 (s, 6H), 1.24 (t, J=7.1 Hz, 3H).

Reference Example 66 3-(Dimethylamino)-2-phenoxypropanoic acid

To a solution of 129 mg (0.544 mmol) of ethyl 3-(dimethylamino)-2-phenoxypropanoate synthesized in the similar manner as in Reference Example 65 in 4 ml of THF, 0.700 ml (0.700 mmol) of a 1 N aqueous sodium hydroxide solution was added with stirring at room temperature and stirred at the same temperature as above for 3 hours.

After the completion of the reaction, 1 N hydrochloric acid was added for neutralization and concentrated under reduced pressure. The operation of adding toluene to the obtained concentration residue and concentrating the resultant under reduced pressure was repeated several times. Dichloromethane was added to the obtained concentration residue and ultrasonicated, then the deposited solid was filtered off, and the filtrate was concentrated under reduced pressure to obtain 75 mg of the title compound (yield: 66%) as a white solid.

Mass spectrum (CI, m/z): 210 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.31-7.22 (m, 2H), 6.96-6.86 (m, 3H), 4.75 (dd, J=5.3, 6.7 Hz, 1H), 3.01 (dd, J=6.7, 13.0 Hz, 1H), 2.95 (dd, J=5.3, 13.0 Hz, 1H), 2.45 (s, 6H).

Reference Example 67 Ethyl 2-bromo-3-(3,3-difluoropyrrolidin-1-yl)propanoate

To a solution of 0.900 g (6.27 mmol) of 3,3-difluoropyrrolidine hydrochloride in 20 ml of dehydrated THF, 1.70 ml (12.1 mmol) of triethylamine was added with stirring at room temperature in an argon atmosphere, and subsequently, a solution of 1.50 g (5.77 mmol) of ethyl 2,3-dibromopropanoate in 20 ml of dehydrated THF was added dropwise at 0° C. and stirred at room temperature for 16 hours.

After the completion of the reaction, precipitates were filtered off, the filtrate was washed with water, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was dried under reduced pressure to obtain 1.30 g of the title compound (yield: 79%) as an orange oil.

Mass spectrum (CI, m/z): 286 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 4.25 (q, J=7.1 Hz, 2H), 4.18 (dd, J=5.8, 9.5 Hz, 1H), 3.27-3.19 (m, 1H), 3.12-2.77 (m, 5H), 2.31-2.16 (m, 2H), 1.30 (t, J=7.1 Hz, 3H).

Reference Example 68 Ethyl 3-(3,3-difluoropyrrolidin-1-yl)-2-phenoxypropanoate

To a solution of 860 mg (9.14 mmol) of phenol in 15 ml of dehydrated DMF, 400 mg (9.17 mmol) of 55% sodium hydride was dividedly added with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 30 minutes. Subsequently, a solution of 1.30 g (4.54 mmol) of ethyl 2-bromo-3-(3,3-difluoropyrrolidin-1-yl)propanoate synthesized in the similar manner as in Reference Example 67 in 10 ml of dehydrated DMF was added dropwise at 0° C. and then stirred at room temperature for 16 hours.

After the completion of the reaction, ice water was added to the reaction solution and then neutralized with 1 N hydrochloric acid, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=100:0 to 70:30 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 476 mg of the title compound (containing impurities) as a pale yellow oil.

Mass spectrum (CI, m/z): 300 [M+1]⁺.

Reference Example 69 3-(3,3-Difluoropyrrolidin-1-yl)-2-phenoxypropanoic acid

To a solution of 476 mg of ethyl 3-(3,3-difluoropyrrolidin-1-yl)-2-phenoxypropanoate (containing impurities) synthesized in Reference Example 68 in 6 ml of THF, 2.00 ml of a 1 N aqueous sodium hydroxide solution was added with stirring at room temperature and stirred at the same temperature as above for 3 hours.

After the completion of the reaction, 1 N hydrochloric acid was added to the reaction solution to adjust the pH to 2, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure to obtain 393 mg of the title compound (containing impurities) as a white foam.

Mass spectrum (CI, m/z): 272 [M+1]⁺.

Reference Example 70 (S)—N-{5-[3-(Benzyloxy)-2-phenylpropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclobutanecarboxamide

To a solution of 168 mg (0.657 mmol) of (S)-3-(benzyloxy)-2-phenylpropanoic acid [synthesized according to the method described in Tetrahedron Lett., 2002 (43), 9691-9693] in 3 ml of dehydrated dichloromethane, 0.10 ml (1.2 mmol) of oxalyl chloride and 0.010 ml (0.13 mmol) of dehydrated DMF were added in this order at 0° C. in a nitrogen atmosphere and then stirred for 3.5 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 127 mg (0.335 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 and 0.23 ml (1.3 mmol) of DIPEA in 3 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added at 0° C. in a nitrogen atmosphere and then stirred for 1 hour with the temperature unchanged. Subsequently, 1.0 ml (7.2 mmol) of triethylamine and 1.0 ml (25 mmol) of methanol were added to the reaction solution at room temperature and then stirred for 19 hours with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution and stirred, followed by extraction with dichloromethane three times. All of the obtained organic layers were dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=80:20 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 142 mg of the title compound (yield: 78%) as a pale yellow foam.

Mass spectrum (CI, m/z): 545 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.43-7.37 (m, 2H), 7.35-7.16 (m, 10H), 4.89 (d, J=12.0 Hz, 1H), 4.59 (d, J=12.0 Hz, 1H), 4.50-4.39 (m, 2H), 4.19-4.12 (m, 1H), 4.05 (dd, J=5.3, 8.6 Hz, 1H), 3.61 (dd, J=5.3, 8.8 Hz, 1H), 2.62-2.49 (m, 2H), 2.33-2.23 (m, 2H), 2.00-1.89 (m, 2H), 1.86 (s, 3H), 1.73 (s, 3H), 0.14 (s, 9H).

Reference Example 71 3-(3-Methoxy-2-phenylpropanoyl)oxazolidin-2-one

To a solution of 506 mg (2.46 mmol) of 3-(2-phenylacetyl)oxazolidin-2-one [synthesized according to the method described in Tetrahedron, 1998 (54) 2697-2708] in 10 ml of dehydrated dichloromethane, 0.33 ml (3.0 mmol) of titanium tetrachloride was added at 0° C. in a nitrogen atmosphere and then stirred for 5 minutes with the temperature unchanged. Subsequently, 0.52 ml (3.0 mmol) of DIPEA was added thereto at 0° C. and then stirred for 1 hour with the temperature unchanged. Subsequently, 0.37 ml (4.9 mmol) of chloromethyl methyl ether was added thereto dropwise at 0° C. and then stirred for 2 hours with the temperature unchanged.

After the completion of the reaction, water was added to the reaction solution at 0° C. and stirred, followed by extraction with dichloromethane three times. All of the obtained organic layers were washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in this order, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=75:25 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 522 mg of the title compound (yield: 85%) as an orange oil.

Mass spectrum (CI, m/z): 250 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.44-7.38 (m, 2H), 7.35-7.27 (m, 3H), 5.38 (dd, J=4.6, 10.2 Hz, 1H), 4.44-4.27 (m, 2H), 4.18-4.07 (m, 2H), 3.95 (ddd, J=6.8, 9.2, 11.0 Hz, 1H), 3.50 (dd, J=4.6, 9.2 Hz, 1H), 3.37 (s, 3H).

Reference Example 72 3-Methoxy-2-phenylpropanoic acid

To a solution of 517 mg (2.07 mmol) of 3-(3-methoxy-2-phenylpropanoyl)oxazolidin-2-one synthesized in the similar manner as in Reference Example 71 in 12 ml of THF/4 ml of water, 1.0 ml (9.7 mmol) of an aqueous hydrogen peroxide solution [30%] at room temperature and 111 mg (4.63 mmol) of lithium hydroxide at 0° C. were added in this order in a nitrogen atmosphere and then stirred for 2.5 hours with the temperature unchanged. Subsequently, 10 ml of a 10% aqueous sodium thiosulfate solution and 10 ml of a saturated aqueous solution of sodium bicarbonate were added in small portions at 0° C. and then stirred at room temperature for 1 hour.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and THF was distilled off. The concentration residue was washed with dichloromethane twice and then adjusted to pH 2 by adding 6 N hydrochloric acid, and subsequently, this solution was subjected to extraction with ethyl acetate three times. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=80:20 to 65:35 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 331 mg of the title compound (yield: 89%) as a colorless oil.

Mass spectrum (CI, m/z): 181 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.38-7.27 (m, 5H), 4.01-3.95 (m, 1H), 3.91 (dd, J=4.8, 9.2 Hz, 1H), 3.63 (dd, J=4.8, 8.7 Hz, 1H), 3.39 (s, 3H).

Reference Example 73 Benzyl 4-methoxy-2-phenylbutanoate

To a solution of 0.45 ml (2.2 mmol) of benzyl phenylacetate in 6 ml of dehydrated DMF, 139 mg (3.19 mmol) of 55% sodium hydride was added at 0° C. in an argon atmosphere and then stirred for 30 minutes with the temperature unchanged. Subsequently, 0.35 ml (3.7 mmol) of 2-bromoethyl methyl ether was added to the reaction solution at 0° C. and then stirred at room temperature for 2 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction with ethyl acetate. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 528 mg of the title compound (yield: 84%) as a colorless oil.

Mass spectrum (ESI, m/z): 285 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.34-7.21 (m, 10H), 5.15 (d, J=12.5 Hz, 1H), 5.05 (d, J=12.5 Hz, 1H), 3.83 (t, J=7.7 Hz, 1H), 3.38-3.30 (m, 1H), 3.29-3.20 (m, 4H), 2.45-2.34 (m, 1H), 2.06-1.95 (m, 1H)

Reference Example 74 4-Methoxy-2-phenylbutanoic acid

To a solution of 528 mg (1.86 mmol) of benzyl 4-methoxy-2-phenylbutanoate synthesized in the similar manner as in Reference Example 73 in 7 ml of ethanol, 130 mg of 10% Pd—C (containing 54.33% water, PE-type manufactured by N.E. Chemcat Corp.) was added at room temperature in an argon atmosphere. After replacement with a hydrogen atmosphere, the resultant was stirred at room temperature for 2 hours.

After the completion of the reaction, the reaction solution was filtered through celite and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=60:40 to 40:60 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 304 mg of the title compound (yield: 84%) as a white solid.

Mass spectrum (CI, m/z): 195 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.37 (br s, 1H), 7.38-7.20 (m, 5H), 3.61 (t, J=7.7 Hz, 1H), 3.29-3.16 (m, 5H), 2.26-2.14 (m, 1H), 1.88-1.77 (m, 1H)

Reference Example 75 (S)—N-{5-[3-(Benzyloxy)-2-phenylpropanoyl]-6,6-dimethyl-1,4,5,6-tetrahydropyrrolo[3,4-c]pyrazol-3-yl}-1-(trimethylsilyl)cyclopropanecarboxamide

To a solution of 51.9 mg (0.202 mmol) of (S)-3-(benzyloxy)-2-phenylpropanoic acid [synthesized according to the method described in Tetrahedron Lett., 2002 (43), 9691-9693] in 2 ml of dehydrated dichloromethane, 0.040 ml (0.47 mmol) of oxalyl chloride and 0.0050 ml (0.065 mmol) of dehydrated DMF were added in this order at 0° C. in a nitrogen atmosphere and then stirred for 2.5 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure to obtain a concentration residue.

To a solution of 47.0 mg (0.129 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclopropanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 46 and 0.10 ml (0.57 mmol) of DIPEA in 1 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 1 ml of dehydrated dichloromethane was added at 0° C. in a nitrogen atmosphere and then stirred for 2 hours with the temperature unchanged. Subsequently, 0.10 ml (0.92 mmol) of N,N-dimethylethane-1,2-diamine was added to the reaction solution at 0° C. and then stirred at room temperature for 3 hours.

After the completion of the reaction, the reaction solution diluted with dichloromethane was washed with a 5% aqueous potassium bisulfate solution and then separated into an aqueous layer and an organic layer. The aqueous layer was subjected to extraction with dichloromethane twice, and then, all of the obtained organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=80:20 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 48 mg of the title compound (yield: 70%) as a pale yellow foam.

Mass spectrum (DUIS, m/z): 531 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.55 (s, 1H), 7.41-7.37 (m, 2H), 7.34-7.20 (m, 9H), 4.84 (d, J=12.0 Hz, 1H), 4.60 (d, J=12.0 Hz, 1H), 4.47 (d, J=12.0 Hz, 1H), 4.42 (d, J=12.0 Hz, 1H), 4.16 (t, J=8.8 Hz, 1H), 4.02 (dd, J=5.4, 8.8 Hz, 1H), 3.61 (dd, J=5.4, 8.8 Hz, 1H), 1.85 (s, 3H), 1.72 (s, 3H), 1.09-1.04 (m, 2H), 0.81-0.76 (m, 2H), 0.10 (s, 9H).

Reference Example 76 (R)-Benzyl 2-ethoxy-2-phenylacetate

To a solution of 1.01 g (4.17 mol) of (R)-benzyl 2-hydroxy-2-phenylacetate in 20 ml (0.25 mol) of iodoethane, 1.93 g (8.33 mmol) of silver oxide was added at room temperature in an argon atmosphere and stirred at 60° C. for 18 hours.

After the completion of the reaction, the reaction solution was filtered through celite, the solid component was washed with ethyl acetate, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 80:20 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 1.03 g of the title compound (yield: 91%) as a colorless oil.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.49-7.43 (m, 2H), 7.38-7.27 (m, 6H), 7.24-7.18 (m, 2H), 5.19 (d, J=12.4 Hz, 1H), 5.11 (d, J=12.4 Hz, 1H), 4.92 (s, 1H), 3.65-3.46 (m, 2H), 1.27 (t, J=7.0 Hz, 3H).

Reference Example 77 (R)-2-Ethoxy-2-phenylacetic acid

To a solution of 1.03 g (3.81 mmol) of (R)-benzyl 2-ethoxy-2-phenylacetate synthesized in the similar manner as in Reference Example 76 in 20 ml of methanol, 0.11 of palladium/carbon (ASCA2 (trade name), manufactured by N.E. Chemcat Corp., containing 54% water) was added in an argon atmosphere and then, after replacement with a hydrogen atmosphere under reduced pressure, stirred at room temperature for 2 hours.

After the completion of the reaction, the reaction solution was filtered through celite, the solid component was washed with methanol, and then, the filtrate was concentrated under reduced pressure to obtain 0.63 g of the title compound (yield: 92%) as a pale yellow oil.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.80 (br s, 1H), 7.44-7.28 (m, 5H), 4.84 (s, 1H), 3.60-3.50 (m, 1H), 3.47-3.20 (m, 1H), 1.15 (t, J=7.0 Hz, 3H).

Reference Example 78 Methyl 2-{[(benzyloxy)carbonyl](2-cyanoethyl)amino}-2-methylpropanoate

To a solution of 5.00 g (29.4 mmol) of methyl 2-[(2-cyanoethyl)amino]-2-methylpropanoate [synthesized according to the method described in J. Med. Chem., 1968, 11 (3), 616-618] in 23 ml of toluene, 15.5 ml (90.7 mol) of DIPEA and 32.0 ml of a solution of 30 to 35% benzyl chloroformate in toluene [purchased from Tokyo Chemical Industry Co., Ltd.)] were added in this order with stirring at room temperature in an argon atmosphere and stirred for 1.5 hours with the temperature unchanged. Subsequently, the resultant was stirred at 50° C. for 1.5 hours and then allowed to cool to room temperature, and 4.80 ml (44.1 mmol) of N,N-dimethylethane-1,2-diamine was added at room temperature and stirred for 2.5 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was poured to 2 N hydrochloric acid and stirred. An aqueous layer and an organic layer were separated, the organic layer was washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in this order, dried over anhydrous magnesium sulfate, and filtered, and then, the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=84:16 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 8.32 g of the title compound (yield: 93%) as a colorless oil.

Mass spectrum (CI, m/z): 305 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.43-7.28 (m, 5H), 5.07 (s, 2H), 3.64 (t, J=6.7 Hz, 2H), 3.50 (br s, 3H), 2.76 (t, J=6.7 Hz, 2H), 1.45 (s, 6H).

Reference Example 79 Benzyl 4-cyano-3-hydroxy-2,2-dimethyl-2,5-dihydro-1H-pyrrole-1-carboxylate

52 ml (52 mmol) of a 1 mol/L solution of potassium tert-butoxide in THF was heated to 60° C., and a solution of 12.1 g (39.7 mmol) of methyl 2-{[(benzyloxy)carbonyl](2-cyanoethyl)amino}-2-methylpropanoate synthesized in the similar manner as in Reference Example 78 in 30 ml of dehydrated THF was added dropwise with stirring under argon stream and stirred for 1 hour while heated to reflux.

After the completion of the reaction, 90 ml of water was added to the reaction solution allowed to cool to room temperature and adjusted to pH<2 by further adding 2 N hydrochloric acid. Extraction was performed from the mixed solution with 100 ml of ethyl acetate twice, and all of the organic layers were combined and washed with 100 ml of water and 100 ml of a saturated aqueous solution of sodium chloride in this order. After drying over magnesium sulfate, filtration and concentration under reduced pressure were performed, and half the amount of the solvent was distilled off. 12 g of active carbon was added to the obtained solution, stirred at room temperature for 30 minutes, filtered, and concentrated under reduced pressure. The obtained concentration residue was diluted with 10 ml of diisopropyl ether, and 50 ml of n-hexane was added thereto and stirred at room temperature for 30 minutes after the deposited solid was disrupted. The solid component was collected by filtration and dried under reduced pressure at 50° C. to obtain 8.27 g of the title compound (yield: 76%) as a pale yellow solid.

Mass spectrum (DUIS, m/z): 273 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.32 (br s, 1H), 7.46-7.25 (m, 5H), 5.18-5.02 (m, 2H), 4.24-4.02 (m, 2H), 1.51-1.35 (m, 6H).

Reference Example 80 Benzyl 3-amino-6,6-dimethyl-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate

To a solution of 200 mg (0.734 mmol) of benzyl 4-cyano-3-hydroxy-2,2-dimethyl-2,5-dihydro-1H-pyrrole-1-carboxylate synthesized in the similar manner as in Reference Example 79 in 5 ml of ethanol, 0.336 ml (5.87 mmol) of acetic acid was added with stirring at room temperature under argon stream and stirred at room temperature for 5 minutes. Subsequently, 0.178 ml (3.66 mmol) of hydrazine monohydrate was added thereto dropwise with stirring at room temperature and stirred for 12 hours under heating to reflux.

After the completion of the reaction, 15 ml of water was added to the reaction solution allowed to cool to room temperature, and then adjusted to pH 8 by adding an aqueous sodium bicarbonate solution. Extraction was performed from the mixed solution with ethyl acetate three times, and all of the organic layers were washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=50:50 to 0:100 (V/V)→1,2-dichloroethane:methanol=80:20 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 141 mg of the title compound (yield: 67%) as a pale yellow foam.

Mass spectrum (CI, m/z): 287 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 11.20 (br s, 1H), 7.45-7.28 (m, 5H), 5.18-5.05 (m, 2H), 5.05-4.77 (m, 2H), 4.28-4.14 (m, 2H), 1.58-1.46 (m, 6H).

Reference Example 81 5-Benzyl 2-ethyl 3-amino-6,6-dimethylpyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate

To a solution of 400 mg (1.40 mmol) of benzyl 3-amino-6,6-dimethyl-4,6-dihydropyrrolo[3,4-c]pyrazole-5(1H)-carboxylate synthesized in the similar manner as in Reference Example 80 in 4 ml of dehydrated THF, 0.594 ml (3.49 mmol) of DIPEA was added with stirring at room temperature under argon stream and stirred at room temperature for 3 minutes. Subsequently, 0.133 ml (1.40 mmol) of ethyl chloroformate was added thereto dropwise with stirring at 0° C. and stirred at 0° C. for 30 minutes.

After the completion of the reaction, water was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate twice. All of the organic layers were washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=71:29 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to respectively obtain 200 mg of the title compound (yield: 40%) as a white foam and 190 mg of an isomer of the title compound (5-benzyl 1-ethyl 3-amino-6,6-dimethylpyrrolo[3,4-c]pyrazole-1,5(4H,6H)-dicarboxylate) (yield: 38%) as a white foam.

Title compound (5-benzyl 2-ethyl 3-amino-6,6-dimethylpyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate)

Mass spectrum (CI, m/z): 359 [M+1]+.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.45-7.29 (m, 5H), 6.63-6.49 (m, 2H), 5.19-5.04 (m, 2H), 4.41-4.30 (m, 2H), 4.28-4.15 (m, 2H), 1.62-1.49 (m, 6H), 1.36-1.28 (m, 3H).

Isomer of the title compound (5-benzyl 1-ethyl 3-amino-6,6-dimethylpyrrolo[3,4-c]pyrazole-1,5(4H,6H)-dicarboxylate)

Mass spectrum (CI, m/z): 359 [M+1]+.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.45-7.29 (m, 5H), 5.78-5.65 (m, 2H), 5.19-5.05 (m, 2H), 4.36-4.17 (m, 4H), 1.79-1.66 (m, 6H), 1.33-1.25 (m, 3H).

Reference Example 82 5-Benzyl 2-ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]pyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate

To a solution of 885 mg (5.14 mmol) of 1-(trimethylsilyl)cyclobutanecarboxylic acid synthesized in the similar manner as in Reference Example 1 in 20 ml of dehydrated dichloromethane, 0.530 ml (6.17 mmol) of oxalyl chloride and 0.020 mL (0.26 mmol) of DMF were added in this order at 0° C. in an argon atmosphere and stirred for 1 hour with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure.

To a solution of 2.25 ml (12.9 mmol) of DIPEA and 920 mg (2.57 mmol) of 5-benzyl 2-ethyl 3-amino-6,6-dimethylpyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate synthesized in the similar manner as in Reference Example 81 in 10 ml of dehydrated dichloromethane, a solution of the obtained concentration residue in 10 ml of dehydrated dichloromethane was added dropwise at 0° C. in an argon atmosphere and then stirred at room temperature for 24 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction from the solution with dichloromethane twice. All of the organic layers were combined, washed with a 5% aqueous potassium bisulfate solution and a saturated aqueous solution of sodium chloride in this order, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 70:30 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 991 mg of the title compound (yield: 75%) as a pale yellow foam.

Mass spectrum (DUIS, m/z): 513 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.78-9.70 (m, 1H), 7.45-7.29 (m, 5H), 5.20-5.08 (m, 2H), 4.63-4.50 (m, 2H), 4.47-4.37 (m, 2H), 2.58-2.41 (m, 2H), 2.31-2.18 (m, 2H), 1.95-1.80 (m, 2H), 1.67-1.51 (m, 6H), 1.39-1.29 (m, 3H), 0.12-0.06 (m, 9H).

Reference Example 83 Ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate

To a solution of 150 mg (0.293 mmol) of 5-benzyl 2-ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]pyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate synthesized in the similar manner as in Reference Example 82 in 4 ml of 2-propanol, 75 mg of 10% palladium/carbon [manufactured by N.E. Chemcat Corp., PE type, containing 50% water] and 1 ml of acetic acid were added in this order at room temperature. After replacement with a hydrogen atmosphere, the resultant was stirred at room temperature for 1 hour.

After the completion of the reaction, the reaction solution was diluted with ethyl acetate and filtered by adding celite. An aqueous sodium bicarbonate solution was added to the filtrate, stirred, and neutralized. This was subjected to extraction with ethyl acetate twice. All of the organic layers were combined, washed with a saturated aqueous solution of sodium bicarbonate, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (elution solvent: 1,2-dichloroethane:methanol=100:0 to 86:14 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 101 mg of the title compound (yield: 91%) as a white foam.

Mass spectrum (DUIS, m/z): 379 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 9.86 (s, 1H), 4.52 (q, J=7.1 Hz, 2H), 4.22 (s, 2H), 2.65-2.52 (m, 2H), 2.38-2.26 (m, 2H), 2.03-1.88 (m, 2H), 1.50-1.43 (m, 9H), 0.15 (s, 9H).

Reference Example 84 Ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate

To a solution of 57.1 g (119 mmol) of 5-tert-butyl 2-ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]pyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate synthesized in the similar manner as in Reference Example 2 in 500 ml of dichloromethane, 28.0 ml (242 mmol) of 2,6-dimethylpyridine and 43.0 ml (238 mmol) of trimethylsilyl trifluoromethanesulfonate were added dropwise in this order at 0° C. in a nitrogen atmosphere and reacted with stirring at 0° C. for 2 hours.

After the completion of the reaction, the reaction solution was poured to 1000 ml of a saturated aqueous solution of sodium bicarbonate, then stirred at room temperature, and subsequently separated into an aqueous layer and an organic layer. The aqueous layer was subjected to extraction with 500 ml of ethyl acetate twice, and then, all of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The operation of adding toluene to the obtained concentration residue and concentrating the resultant under reduced pressure was performed three times, then the obtained brown oil was refrigerated overnight, and subsequently, 50 ml of diethyl ether and 100 ml of n-hexane were added and stirred at room temperature for 0.5 hours. The deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 17.0 g of the title compound (yield: 38%) as a white solid.

Mass spectrum (DUIS, m/z): 379 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 9.86 (s, 1H), 4.52 (q, J=7.1 Hz, 2H), 4.23 (s, 2H), 2.64-2.52 (m, 2H), 2.38-2.27 (m, 2H), 2.03-1.89 (m, 2H), 1.53-1.42 (m, 9H), 0.14 (s, 9H).

Reference Example 85 (R)-Benzyl 2-cyclopropoxy-2-phenylacetate

To a solution of 7.50 ml (7.50 mmol) of a 1 M solution of diethylzinc in n-hexane in 4 ml of dehydrated dichloromethane, a solution of 0.750 ml (9.31 mmol) of diiodomethane in 1 ml of dehydrated dichloromethane was added dropwise with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 30 minutes. Subsequently, a solution of 500 mg (1.86 mmol) of (R)-benzyl 2-phenyl-2-(vinyloxy)acetate [synthesized according to the method described in J. Am. Chem. Soc., 2006, 128, 2587-2593] in 1 ml of dehydrated dichloromethane was added dropwise with stirring at 0° C. and stirred at room temperature for 6 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction with dichloromethane. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 80:20 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 416 mg of the title compound (yield: 79%) as a colorless oil.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.47-7.41 (m, 2H), 7.38-7.28 (m, 6H), 7.25-7.20 (m, 2H), 5.20 (d, J=12.5 Hz, 1H), 5.12 (d, J=12.5 Hz, 1H), 5.01 (s, 1H), 3.43 (tt, J=3.0, 6.1 Hz, 1H), 0.76-0.65 (m, 2H), 0.53-0.43 (m, 2H).

Reference Example 86 (R)-2-Cyclopropoxy-2-phenylacetic acid

To a solution of 416 mg (1.47 mmol) of (R)-benzyl 2-cyclopropoxy-2-phenylacetate synthesized in the similar manner as in Reference Example 85 in 2 ml of methanol/2 ml of water, 93 mg (2.2 mmol) of lithium hydroxide monohydrate was added at room temperature and then reacted with stirring at room temperature for 2 hours.

After the completion of the reaction, diethyl ether was added to the reaction solution and then the aqueous layer and the organic layer were separated. The aqueous layer was adjusted to pH 2 by adding 2 N hydrochloric acid, followed by extraction with ethyl acetate three times. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to obtain 274 mg of the title compound (yield: 97%) as a colorless oil.

Mass spectrum (DUIS, m/z): 191 [M−1]⁻.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.48-7.32 (m, 5H), 4.99 (s, 1H), 3.43 (tt, J=2.9, 6.0 Hz, 1H), 0.76-0.64 (m, 2H), 0.61-0.43 (m, 2H).

Reference Example 87 (R)-2-Isopropoxy-2-phenylacetic acid

To a suspension of 1.46 g (6.03 mmol) of (R)-benzyl 2-hydroxy-2-phenylacetate in 14.0 ml (140 mmol) of 2-iodopropane, 2.79 g (12.0 mmol) of silver(I) oxide was added at room temperature in an argon atmosphere and then reacted with stirring for 14.5 hours under heating to reflux.

After the completion of the reaction, the reaction solution was allowed to cool to room temperature and then filtered using a celite filter. The filtration cake was washed with ethyl acetate, and then, all of the filtrates were concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=95:5 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 675 mg of a concentration residue.

To a solution of the obtained concentration residue in 10 ml of methanol/2.0 ml of water, 176 mg (4.19 mmol) of lithium hydroxide monohydrate was added at room temperature in an argon atmosphere and then reacted with stirring at room temperature for 4 hours.

After the completion of the reaction, water and diethyl ether were added to the reaction solution, stirred, and then the aqueous layer and the organic layer were separated. The aqueous layer was adjusted to pH 2 by adding 2 N hydrochloric acid, followed by extraction with ethyl acetate three times. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=85:15 to 70:30 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 467 mg of a concentration residue. The obtained concentration residue was subjected to preparative HPLC (column: X-Bridge (trade name) ODS, elution solvent: 1 vol % formic acid/acetonitrile:1 vol % aqueous formic acid solution=20:80 to 70:30 (V/V)), a fraction containing the compound of interest was concentrated under reduced pressure, and acetonitrile was distilled off. The obtained concentration residue was subjected to extraction with ethyl acetate three times, and subsequently, all of the organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and dried under reduced pressure to obtain 346 mg of the title compound (yield: 30% [2 steps]) as a white solid.

Mass spectrum (CI, m/z): 195 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.74 (br s, 1H), 7.43-7.27 (m, 5H), 4.95 (s, 1H), 3.62 (spt, J=6.1 Hz, 1H), 1.15 (d, J=6.1 Hz, 3H), 1.09 (d, J=6.1 Hz, 3H).

Reference Example 88 (R)-Ethyl 2-phenyl-2-(trifluoromethoxy)acetate

To a solution of 25.0 g (139 mmol) of (R)-ethyl 2-hydroxy-2-phenylacetate in 10 ml of deuterated chloroform, 3.75 g (4.75 mmol) of 40% 1-trifluoromethyl-3,3-dimethyl-1,2-benziodoxole [Togni Reagent II (trade name), diatomaceous earth mixture, purchased from Tokyo Chemical Industry Co., Ltd.] and 0.900 g (1.44 mmol) of bis(trifluoromethylsulfonyl)imide zinc(II) were added with stirring at room temperature in an argon atmosphere and stirred at room temperature for 88 hours.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate was added to the reaction solution, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 60:40 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 421 mg of the title compound (containing impurities) as a yellow oil.

Mass spectrum (CI, m/z): 249 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.53-7.36 (m, 5H), 5.52 (s, 1H), 4.32-4.16 (m, 2H), 1.25 (t, J=7.1 Hz, 3H).

Reference Example 89 (R)-2-Phenyl-2-(trifluoromethoxy)acetic acid

To a solution of 421 mg of (R)-ethyl 2-phenyl-2-(trifluoromethoxy)acetate (containing impurities) synthesized in the similar manner as in Reference Example 88 in 3 ml of methanol/3 ml of water, 93 mg (2.2 mmol) of lithium hydroxide monohydrate was added at room temperature and then reacted with stirring at room temperature for 4 hours.

After the completion of the reaction, diethyl ether was added to the reaction solution and then the aqueous layer and the organic layer were separated. The aqueous layer was adjusted to pH 2 by adding 2 N hydrochloric acid, followed by extraction with ethyl acetate three times. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to obtain 390 mg of the title compound (containing impurities) as a pale yellow oil.

Mass spectrum (DUIS, m/z): 219 [M−1]⁻.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.52-7.37 (m, 5H), 5.57 (s, 1H).

Reference Example 90 (R)-Benzyl 2-phenyl-2-propoxyacetate

To a suspension of 1.58 g (6.52 mmol) of (R)-benzyl 2-hydroxy-2-phenylacetate in 14.5 ml (149 mmol) of 1-iodopropane, 3.03 g (13.1 mmol) of silver(I) oxide was added at room temperature in an argon atmosphere and then reacted with stirring at 80° C. for 14 hours.

After the completion of the reaction, the reaction solution was allowed to cool to room temperature and then filtered using a celite filter. The filtration cake was washed with ethyl acetate, and then, all of the filtrates were concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=97:3 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 1.23 g of the title compound (yield: 66%) as a colorless oil.

Mass spectrum (CI, m/z): 285 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.43-7.27 (m, 8H), 7.26-7.20 (m, 2H), 5.13 (s, 2H), 5.06 (s, 1H), 3.46 (td, J=6.6, 9.0 Hz, 1H), 3.40-3.28 (m, 1H), 1.60-1.49 (m, 2H), 0.85 (t, J=7.4 Hz, 3H).

Reference Example 91 (R)-2-Phenyl-2-propoxyacetic acid

To a solution of 1.23 g (4.33 mmol) of (R)-benzyl 2-phenyl-2-propoxyacetate synthesized in the similar manner as in Reference Example 90 in 15 ml of ethanol, 274 mg of 10% palladium/carbon [PE type (trade name), manufactured by N.E. Chemcat Corp., containing 54% water] was added at room temperature in an argon atmosphere and then, after replacement with a hydrogen atmosphere under reduced pressure, reacted with stirring at room temperature for 1.5 hours.

After the completion of the reaction, the inside of the reaction container was replaced with an argon atmosphere under reduced pressure. The reaction solution was filtered using a celite filter, the removed solid was washed with ethanol, and then, the filtrate was concentrated under reduced pressure and dried under reduced pressure to obtain 892 mg of the title compound (containing impurities) as a colorless oil.

Mass spectrum (CI, m/z): 195 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 12.78 (br s, 1H), 7.42-7.29 (m, 5H), 4.83 (s, 1H), 3.47 (td, J=6.6, 9.0 Hz, 1H), 3.40-3.25 (m, 1H), 1.61-1.49 (m, 2H), 0.87 (t, J=7.4 Hz, 3H).

Reference Example 92 Methyl 2-(4-fluorophenyl)-2-methoxyacetate

To a solution of 800 mg (4.70 mmol) of 4-fluoromandelic acid in 20 ml of dehydrated DMF, 450 mg (10.3 mmol) of 55% sodium hydride was dividedly added with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 1 hour. Subsequently, 0.732 ml (11.8 mmol) of iodomethane was added dropwise at 0° C. and then stirred at room temperature for 2 hours. 0.732 ml (11.8 mmol) of iodomethane was further added dropwise at 0° C. and then stirred at room temperature for 2 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 70:30 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 247 mg of the title compound (yield: 27%) as a colorless oil.

Mass spectrum (CI, m/z): 199 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.46-7.38 (m, 2H), 7.11-7.02 (m, 2H), 4.76 (s, 1H), 3.73 (s, 3H), 3.40 (s, 3H).

Reference Example 93 2-(4-Fluorophenyl)-2-methoxyacetic acid

To a solution of 247 mg (1.25 mmol) of methyl 2-(4-fluorophenyl)-2-methoxyacetate synthesized in the similar manner as in Reference Example 92 in 5 ml of THF, 2.0 ml (2.0 mmol) of a 1 N aqueous sodium hydroxide solution was added with stirring at room temperature and stirred at the same temperature as above for 16 hours.

After the completion of the reaction, 1 N hydrochloric acid was added to the reaction solution to adjust the pH to 2, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure and dried under reduced pressure to obtain 260 mg of the title compound (containing impurities) as a brown oil.

Mass spectrum (CI, m/z): 185 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.49-7.36 (m, 2H), 7.13-7.03 (m, 2H), 4.77 (s, 1H), 3.43 (s, 3H).

Reference Example 94 Ethyl 2-(3-fluorophenyl)-2-hydroxyacetate

To a suspension of 1.00 g (7.15 mmol) of 3-fluorophenylboronic acid in 30 ml of dehydrated toluene, 2.20 g (10.8 mmol) of a solution of 50% ethyl oxoacetate in toluene [purchased from Apollo scientific limited] and 107 mg (0.359 mmol) of 2-(di-tert-butylphosphino)biphenyl were added with stirring at room temperature in an argon atmosphere, followed by replacement with a nitrogen atmosphere under reduced pressure. Subsequently, 92.0 mg (0.100 mmol) of tris(dibenzylideneacetone)dipalladium(0) was added with stirring at room temperature and reacted at 80° C. for 9 hours.

The reaction solution was filtered using a celite filter, and water was added to the filtrate, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 60:40 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 263 mg of the title compound (yield: 19%) as a pale yellow oil.

Mass spectrum (CI, m/z): 199 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.38-7.29 (m, 1H), 7.25-7.20 (m, 1H), 7.19-7.13 (m, 1H), 7.06-6.98 (m, 1H), 5.15 (d, J=5.4 Hz, 1H), 4.34-4.14 (m, 2H), 3.50 (d, J=5.4 Hz, 1H), 1.25 (t, J=7.2 Hz, 3H).

Reference Example 95 Ethyl 2-(3-fluorophenyl)-2-methoxyacetate

To a solution of 263 mg (1.33 mmol) of ethyl 2-(3-fluorophenyl)-2-hydroxyacetate synthesized in the similar manner as in Reference Example 94 in 8.0 ml (130 mmol) of iodomethane, 615 mg (2.65 mmol) of silver oxide was added at room temperature in an argon atmosphere and reacted with stirring at the same temperature as above for 3 hours.

After the completion of the reaction, the resultant was filtered using a celite filter, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 60:40 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 155 mg of the title compound (yield: 55%) as a colorless oil.

Mass spectrum (CI, m/z): 213 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.37-7.29 (m, 1H), 7.25-7.15 (m, 2H), 7.07-7.00 (m, 1H), 4.75 (s, 1H), 4.28-4.12 (m, 2H), 3.43 (s, 3H), 1.23 (t, J=7.1 Hz, 3H).

Reference Example 96 2-(3-Fluorophenyl)-2-methoxyacetic acid

To a solution of 155 mg (0.730 mmol) of ethyl 2-(3-fluorophenyl)-2-methoxyacetate synthesized in the similar manner as in Reference Example 95 in 5 ml of THF, 1.0 ml (1.0 mmol) of a 1 N aqueous sodium hydroxide solution was added with stirring at room temperature and stirred at the same temperature as above for 20 hours.

After the completion of the reaction, 1 N hydrochloric acid was added to the reaction solution to adjust the pH to 2, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure to obtain 144 mg of the title compound (containing impurities) as a colorless oil.

Mass spectrum (CI, m/z): 185 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.41-7.32 (m, 1H), 7.25-7.20 (m, 1H), 7.19-7.13 (m, 1H), 7.10-7.03 (m, 1H), 4.79 (s, 1H), 3.46 (s, 3H).

Reference Example 97 (R)-Methyl 2-(2-fluorophenyl)-2-methoxyacetate

To a solution of 1.00 g (5.88 mmol) of (R)-2-(2-fluorophenyl)-2-hydroxyacetic acid [purchased from Combi-Blocks Inc.] in 20 ml of dehydrated DMF, 310 mg (7.10 mmol) of 55% sodium hydride was dividedly added with stirring at 0° C. in an argon atmosphere and stirred at the same temperature as above for 1 hour. Subsequently, 0.842 ml (13.5 mmol) of iodomethane was added dropwise at 0° C. and then stirred at room temperature for 4 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 70:30 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 858 mg of the title compound (yield: 74%) as a colorless oil.

Mass spectrum (CI, m/z): 199 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.50-7.42 (m, 1H), 7.38-7.30 (m, 1H), 7.21-7.14 (m, 1H), 7.13-7.05 (m, 1H), 5.14 (s, 1H), 3.43 (s, 3H).

Reference Example 98 (R)-2-(2-Fluorophenyl)-2-methoxyacetic acid

To a solution of 858 mg (4.33 mmol) of (R)-methyl 2-(2-fluorophenyl)-2-methoxyacetate synthesized in the similar manner as in Reference Example 97 in 10 ml of THF, 5.2 ml (5.2 mmol) of a 1 N aqueous sodium hydroxide solution was added with stirring at room temperature and stirred at 50° C. for 3 hours.

After the completion of the reaction, the resultant was allowed to cool to room temperature, and then, 1 N hydrochloric acid was added to the reaction solution to adjust the pH to 2, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure to obtain 390 mg of the title compound (yield: 49%) as a brown oil.

Mass spectrum (CI, m/z): 185 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.46-7.32 (m, 2H), 7.22-7.05 (m, 2H), 5.11 (s, 1H), 3.43 (s, 3H).

Reference Example 99 Ethyl 2-hydroxy-2-(thiophen-2-yl)acetate

To a suspension of 1.00 g (7.82 mmol) of thiophene-2-boronic acid in 30 ml of dehydrated toluene, 2.40 g (11.8 mmol) of a solution of 50% ethyl oxoacetate in toluene [purchased from Apollo scientific limited] and 117 mg (0.392 mmol) of 2-(di-tert-butylphosphino)biphenyl were added with stirring at room temperature in an argon atmosphere, followed by replacement with a nitrogen atmosphere under reduced pressure. Subsequently, 101 mg (0.110 mmol) of tris(dibenzylideneacetone)dipalladium(0) was added with stirring at room temperature and reacted at 80° C. for 9 hours.

The reaction solution was filtered using a celite filter, and water was added to the filtrate, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 60:40 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 86 mg of the title compound (yield: 6%) as a yellow oil.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.29 (dd, J=1.2, 5.1 Hz, 1H), 7.13-7.09 (m, 1H), 7.00 (dd, J=3.6, 5.1 Hz, 1H), 5.43-5.37 (m, 1H), 4.37-4.22 (m, 2H), 3.48 (d, J=6.4 Hz, 1H), 1.30 (t, J=7.2 Hz, 3H).

Reference Example 100 Ethyl 2-methoxy-2-(thiophen-2-yl)acetate

To a solution of 86 mg (0.46 mmol) of ethyl 2-hydroxy-2-(thiophen-2-yl)acetate synthesized in the similar manner as in Reference Example 99 in 4.0 ml (64 mmol) of iodomethane, 214 mg (0.923 mmol) of silver oxide was added at room temperature in an argon atmosphere and reacted with stirring at the same temperature as above for 3 hours.

After the completion of the reaction, the resultant was filtered using a celite filter, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 60:40 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 68.5 mg of the title compound (yield: 74%) as a colorless oil.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.33 (dd, J=1.2, 5.1 Hz, 1H), 7.16-7.10 (m, 1H), 7.00 (dd, J=3.5, 5.1 Hz, 1H), 5.02 (s, 1H), 4.33-4.17 (m, 2H), 3.44 (s, 3H), 1.28 (t, J=7.2 Hz, 3H).

Reference Example 101 2-Methoxy-2-(thiophen-2-yl)acetic acid

To a solution of 68 mg (0.34 mmol) of ethyl 2-methoxy-2-(thiophen-2-yl)acetate synthesized in the similar manner as in Reference Example 100 in 3 ml of THF, 0.5 ml (0.5 mmol) of a 1 N aqueous sodium hydroxide solution was added with stirring at room temperature and stirred at the same temperature as above for 16 hours.

After the completion of the reaction, 1 N hydrochloric acid was added to the reaction solution to adjust the pH to 2, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure and dried under reduced pressure to obtain 60 mg of the title compound (containing impurities) as a pale yellow oil.

Mass spectrum (DUIS, m/z): 171 [M−1]⁻.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.36 (dd, J=1.2, 5.1 Hz, 1H), 7.19-7.14 (m, 1H), 7.02 (dd, J=3.5, 5.1 Hz, 1H), 5.07 (s, 1H), 3.48 (s, 3H).

Reference Example 102 Mixture of 2-ethyl 5-(trichloromethyl) 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]pyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate, and ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate

To a solution of 8.03 g (21.2 mmol) of ethyl 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 84 in 100 ml of dehydrated dichloromethane, 12.9 ml (74.1 mmol) of DIPEA was added at room temperature in an argon atmosphere. Subsequently, a solution of 4.40 g (14.8 mmol) of bis(trichloromethyl)carbonate in 10 ml of dehydrated dichloromethane was added dropwise at −78° C. and then stirred for 1.5 hours with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of sodium bicarbonate and dichloromethane were added to the reaction solution and then stirred for 1 hour while the temperature was raised to room temperature for a while. The reaction solution was separated into an aqueous layer and an organic layer, and then, the aqueous layer was subjected to extraction with ethyl acetate twice. All of the organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=85:15→75:25 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure. n-Hexane was added to the obtained concentration residue, stirred at room temperature for 10 minutes, and then left standing for 15 minutes in a freezer. The deposited solid was filtered off, and the filtrate obtained by washing the removed solid with n-hexane was concentrated under reduced pressure and dried under reduced pressure to obtain a mixture of 2.90 g of 2-ethyl 5-(trichloromethyl) 6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]pyrrolo[3,4-c]pyrazole-2,5(4H,6H)-dicarboxylate (yield: 25%) and 1.75 g of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate (yield: 19%) as a white foam.

Mass spectrum (ESI, m/z): 539 [M+1]⁺, 441 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 9.99-9.84 (m, total 1H), 4.97 (s, 0.85H), 4.84-4.79 (m, total 1.15H), 4.59-4.51 (m, total 2H), 2.64-2.53 (m, total 2H), 2.39-2.28 (m, total 2H), 2.03-1.92 (m, total 2H), 1.82-1.75 (m, total 6H), 1.51-1.44 (m, total 3H), 0.19-0.13 (m, total 9H).

Reference Example 103 {1-[Amino(phenyl)methyl]cyclobutyl}methanol

To a solution of 2.07 g (23.2 mmol) of ethyl carbamate in 20 ml of toluene, 2.36 ml (23.2 mmol) of benzaldehyde and 235 mg (1.23 mmol) of p-toluenesulfonic acid monohydrate were added in this order at room temperature in an argon atmosphere and then stirred at room temperature for 5 minutes. Subsequently, 1.80 ml (23.2 mmol) of cyclobutanecarbaldehyde was added at room temperature and then stirred at 60° C. for 4 hours.

After the completion of the reaction, the reaction solution was poured to a saturated aqueous solution of sodium bicarbonate and then stirred at room temperature. After separation into an aqueous layer and an organic layer, the aqueous layer was subjected to extraction with toluene once. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 60:40 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 2.20 g of a concentration residue.

To a solution of the obtained concentration residue in 10 ml of ethanol, 199 mg (5.26 mmol) of sodium borohydride was dividedly added at 0° C. in an argon atmosphere and then stirred at 0° C. for 0.5 hours and further at room temperature for 2.5 hours. Subsequently, 990 mg (17.7 mmol) of potassium hydroxide and 5.0 ml of water were added to the reaction solution at room temperature and then stirred for 2.5 hours under heating to reflux.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and ethanol was distilled off. 2 N hydrochloric acid was added to the concentration residue and then washed with diethyl ether. After separation into an aqueous layer and an organic layer, the obtained aqueous layer was adjusted to pH>10 by adding a 2 N aqueous sodium hydroxide solution, followed by extraction with dichloromethane three times. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was dissolved in 1,2-dichloroethane, then n-hexane was added, and the deposited solid was collected by filtration, washed with n-hexane, and then dried under reduced pressure to obtain 859 mg of the title compound (yield: 19% [2 steps]) as a white solid.

Mass spectrum (CI, m/z): 192 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.36-7.25 (m, 4H), 7.24-7.16 (m, 1H), 3.97 (s, 1H), 3.41 (d, J=10.7 Hz, 1H), 3.25 (d, J=10.7 Hz, 1H), 2.06-1.92 (m, 2H), 1.79-1.63 (m, 2H), 1.61-1.50 (m, 1H), 1.47-1.37 (m, 1H).

Reference Example 104 (R)—N-[2-(1-Hydroxycyclopropyl)-1-phenylethyl]-2,2,2-trifluoroacetamide

To a solution of 1.01 g (3.67 mmol) of (R)-methyl 3-phenyl-3-(2,2,2-trifluoroacetamido)propanoate synthesized in the similar manner as in Reference Example 22 in 10 ml of dehydrated THF, 0.22 ml (0.75 mmol) of tetraisopropyl orthotitanate was added at 0° C. in an argon atmosphere, and then, 11.0 ml (11.0 mmol) of 1 M ethyl magnesium bromide/THF solution was added dropwise at 0° C. over 1 hour and then stirred for 3 hours with the temperature unchanged and subsequently for 1.5 hours after the temperature was raised to room temperature.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution and stirred, and then, insoluble matter was filtered off using a celite filter. The solid collected by filtration was washed with ethyl acetate, and then, the filtrate was separated into an aqueous layer and an organic layer. The aqueous layer was subjected to extraction with ethyl acetate once, and then, all of the organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=95:5 to 75:25 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 489 mg of the title compound (yield: 49%) as a pale yellow solid.

Mass spectrum (CI, m/z): 274 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.67 (br s, 1H), 7.37-7.30 (m, 4H), 7.30-7.21 (m, 1H), 5.33-5.05 (m, 2H), 2.01 (dd, J=5.2, 14.2 Hz, 1H), 1.93 (dd, J=9.2, 14.2 Hz, 1H), 0.57-0.46 (m, 2H), 0.45-0.37 (m, 1H), 0.11-0.04 (m, 1H).

Reference Example 105 (R)-1-(2-Amino-2-phenylethyl)cyclopropanol

To a solution of 412 mg (1.51 mmol) of (R)—N-[2-(1-hydroxycyclopropyl)-1-phenylethyl]-2,2,2-trifluoroacetamide synthesized in the similar manner as in Reference Example 104 in 7 ml of ethanol, 174 mg (4.60 mmol) of sodium borohydride was added at room temperature in an argon atmosphere and then stirred at room temperature for 14.5 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution at 0° C. and then stirred at room temperature. Insoluble matter was dissolved by adding water, followed by extraction with dichloromethane twice. All of the organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=75:25 to 60:40 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 259 mg of the title compound (containing impurities) as a pale yellow solid.

Mass spectrum (CI, m/z): 178 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.38-7.24 (m, 4H), 7.21-7.14 (m, 1H), 4.15 (dd, J=4.0, 9.4 Hz, 1H), 1.82 (ddd, J=1.3, 9.4, 13.9 Hz, 1H), 1.51-1.44 (m, 1H), 0.58-0.51 (m, 1H), 0.49-0.42 (m, 1H), 0.41-0.34 (m, 1H), 0.21-0.14 (m, 1H).

Reference Example 106 (R)—N-(3-Ethyl-3-hydroxy-1-phenylpentyl)-2,2,2-trifluoroacetamide

To a solution of 700 mg (2.54 mmol) of (R)-methyl 3-phenyl-3-(2,2,2-trifluoroacetamido)propanoate synthesized in the similar manner as in Reference Example 22 in 10 ml of dehydrated THF, 7.63 ml (7.63 mmol) of 1 M ethyl magnesium bromide-THF solution was added dropwise at 0° C. in an argon atmosphere and then stirred at room temperature for 6 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction with ethyl acetate. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 714 mg of the title compound (containing impurities) as a colorless oil.

Mass spectrum (CI, m/z): 304 [M+1]⁺.

Reference Example 107 (R)-1-Amino-3-ethyl-1-phenylpentan-3-ol

To a solution of 714 mg of (R)—N-(3-ethyl-3-hydroxy-1-phenylpentyl)-2,2,2-trifluoroacetamide (containing impurities) synthesized in Reference Example 106 in 1 ml of water/5 ml of methanol, 651 mg (4.71 mmol) of potassium carbonate was added at room temperature in an argon atmosphere and then stirred for 20 hours with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction with ethyl acetate. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=75:25 to 60:40 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 120 mg of the title compound (yield: 23% [2 steps]) as a colorless oil.

Mass spectrum (CI, m/z): 208 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.38-7.25 (m, 4H), 7.22-7.15 (m, 1H), 4.01 (dd, J=2.6, 10.9 Hz, 1H), 1.66-1.41 (m, 4H), 1.38-1.25 (m, 2H), 0.86-0.71 (m, 6H)

Reference Example 108 (E)-Methyl 3-(4-fluorophenyl)acrylate

To a solution of 2.0 g (16 mmol) of 4-fluorobenzaldehyde in 20 ml of dehydrated THF, 6.47 g (19.4 mmol) of methyl 2-(triphenylphosphoranylidene)acetate was added at room temperature in an argon atmosphere and then stirred for 20 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. 20 ml of TBME was added to the obtained concentration residue and filtered, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 90:10 (v/v)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 2.74 g of the title compound (yield: 94%) as a white solid.

Mass spectrum (CI, m/z): 181 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.66 (d, J=16.0 Hz, 1H), 7.55-7.47 (m, 2H), 7.13-7.03 (m, 2H), 6.41-6.33 (m, 1H), 3.81 (s, 3H).

Reference Example 109 (R)-Methyl 3-{benzyl[(S)-1-phenylethyl]amino}-3-(4-fluorophenyl)propanoate

To a solution of 2.79 ml (13.3 mmol) of (S)—N-benzyl-1-phenylethanamine in 30 ml of dehydrated THF, 7.80 ml (12.5 mmol) of a 1.6 M solution of n-butyllithium in n-hexane was added dropwise at −78° C. in an argon atmosphere and then stirred for 30 minutes with the temperature unchanged. Subsequently, a solution of 1.5 g (8.3 mmol) of (E)-methyl 3-(4-fluorophenyl)acrylate synthesized in the similar manner as in Reference Example 108 in 5 ml of THF was added at −78° C. and then stirred for 1 hour with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 1.53 g of the title compound (yield: 47%) as a pale yellow oil.

Mass spectrum (CI, m/z): 392 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.43-7.16 (m, 12H), 7.08-6.96 (m, 2H), 4.42 (dd, J=5.4, 9.7 Hz, 1H), 3.97 (q, J=6.9 Hz, 1H), 3.72 (d, J=14.7 Hz, 1H), 3.65 (d, J=14.7 Hz, 1H), 3.47 (s, 3H), 2.65 (dd, J=5.4, 14.9 Hz, 1H), 2.52 (dd, J=9.7, 14.9 Hz, 1H), 1.27-1.21 (m, 3H).

Reference Example 110 (R)-4-{Benzyl[(S)-1-phenylethyl]amino}-4-(4-fluorophenyl)-2-methylbutan-2-ol

To a solution of 1.35 g (3.45 mmol) of (R)-methyl 3-{benzyl[(S)-1-phenylethyl]amino}-3-(4-fluorophenyl)propanoate synthesized in the similar manner as in Reference Example 109 in 20 ml of dehydrated THF, 10.4 ml (10.4 mmol) of 1 M methyl magnesium bromide-THF solution was added dropwise at 0° C. under argon stream and then stirred at room temperature for 20 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=95:5 to 85:15 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 850 mg of the title compound (yield: 63%) as a colorless oil.

Mass spectrum (ESI, m/z): 392 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.48-7.09 (m, 14H), 4.21 (s, 1H), 4.09-3.98 (m, 1H), 3.92-3.85 (m, 1H), 3.74 (d, J=15.1 Hz, 1H), 3.63 (d, J=15.1 Hz, 1H), 2.10 (dd, J=9.2, 13.9 Hz, 1H), 2.02-1.93 (m, 1H), 0.93 (d, J=6.8 Hz, 3H), 0.82 (s, 3H), 0.69 (s, 3H).

Reference Example 111 (R)-4-Amino-4-(4-fluorophenyl)-2-methylbutan-2-ol

To a solution of 850 mg (2.17 mmol) of (R)-4-{benzyl[(S)-1-phenylethyl]amino}-4-(4-fluorophenyl)-2-methylbutan-2-ol synthesized in the similar manner as in Reference Example 110 in 10 ml of methanol, 425 mg of 20% palladium hydroxide/carbon (containing 50% water) was added at room temperature under argon stream and after replacement with a hydrogen atmosphere, stirred at room temperature for 7 hours.

After the completion of the reaction, the reaction solution was diluted with ethyl acetate and filtered through celite. The filtrate was concentrated under reduced pressure, the obtained concentration residue was subjected to silica gel column chromatography (DIOL, elution solvent: n-hexane:ethyl acetate=75:25 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 248 mg of the title compound (containing impurities) as a colorless oil.

Mass spectrum (CI, m/z): 198 [M+1]⁺.

Reference Example 112 (E)-Methyl 3-(3-fluorophenyl)acrylate

To a solution of 1.27 ml (12.1 mmol) of 3-fluorobenzaldehyde in 25 ml of dehydrated THF, 5.25 g (15.7 mmol) of methyl 2-(triphenylphosphoranylidene)acetate was added at room temperature under argon stream and then stirred for 16 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. 20 ml of TBME was added to the obtained concentration residue, insoluble matter was filtered off, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 1.75 g of the title compound (yield: 80%) as a colorless oil.

Mass spectrum (CI, m/z): 181 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.65 (d, J=16.1 Hz, 1H), 7.40-7.33 (m, 1H), 7.32-7.27 (m, 1H), 7.25-7.19 (m, 1H), 7.12-7.05 (m, 1H), 6.44 (d, J=16.1 Hz, 1H), 3.82 (s, 3H).

Reference Example 113 (R)-Methyl 3-{benzyl [(S)-1-phenylethyl]amino}-3-(3-fluorophenyl)propanoate

To a solution of 3.25 ml (15.5 mmol) of (S)—N-benzyl-1-phenylethanamine in 30 ml of dehydrated THF, 9.11 ml (14.6 mmol) of a 1.6 M solution of n-butyllithium in n-hexane was added dropwise at −78° C. in an argon atmosphere and then stirred for 1 hour with the temperature unchanged. Subsequently, a solution of 1.75 g (9.71 mmol) of (E)-methyl 3-(3-fluorophenyl)acrylate synthesized in the similar manner as in Reference Example 112 in 5 ml of THF was added at −78° C. and then stirred for 1 hour with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 2.22 g of the title compound (yield: 58%) as a pale yellow oil.

Mass spectrum (CI, m/z): 392 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.45-7.09 (m, 13H), 7.00-6.91 (m, 1H), 4.44 (dd, J=5.4, 9.4 Hz, 1H), 3.98 (q, J=6.9 Hz, 1H), 3.73 (d, J=14.6 Hz, 1H), 3.66 (d, J=14.6 Hz, 1H), 3.49 (s, 3H), 2.63 (dd, J=5.4, 15.2 Hz, 1H), 2.54 (dd, J=9.4, 15.2 Hz, 1H), 1.25 (d, J=6.9 Hz, 3H).

Reference Example 114 (R)-4-{Benzyl [(S)-1-phenylethyl]amino}-4-(3-fluorophenyl)-2-methylbutan-2-ol

To a solution of 2.22 g (5.67 mmol) of (R)-methyl 3-{benzyl[(S)-1-phenylethyl]amino}-3-(3-fluorophenyl)propanoate synthesized in the similar manner as in Reference Example 113 in 20 ml of dehydrated THF, 17.0 ml (17.0 mmol) of 1 M methyl magnesium bromide-THF solution was added dropwise at 0° C. in an argon atmosphere and then stirred at room temperature for 17 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=95:5 to 85:15 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 1.95 g of the title compound (yield: 88%) as a colorless oil.

Mass spectrum (CI, m/z): 392 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.42-7.22 (m, 11H), 7.20-7.15 (m, 1H), 7.13-7.07 (m, 1H), 7.06-6.99 (m, 1H), 5.45 (s, 1H), 4.32-4.20 (m, 2H), 4.17-4.05 (m, 1H), 3.61 (d, J=13.2 Hz, 1H), 2.39 (dd, J=10.6, 14.7 Hz, 1H), 1.40 (dd, J=3.4, 14.7 Hz, 1H), 1.12 (s, 3H), 1.03 (d, J=7.0 Hz, 3H), 0.62 (s, 3H).

Reference Example 115 (R)-4-Amino-4-(3-fluorophenyl)-2-methylbutan-2-ol

To a solution of 1.1 g (2.8 mmol) of (R)-4-{benzyl[(S)-1-phenylethyl]amino}-4-(3-fluorophenyl)-2-methylbutan-2-ol synthesized in the similar manner as in Reference Example 114 in 10 ml of methanol, 200 mg of 20% palladium hydroxide/carbon (containing 50% water) was added at room temperature under argon stream and after replacement with a hydrogen atmosphere, stirred at room temperature for 6 hours. Subsequently, after replacement with an argon atmosphere, 0.354 g (5.61 mmol) of ammonium formate was added at room temperature and stirred at 60° C. for 2 hours.

After the completion of the reaction, the reaction solution was diluted with ethyl acetate and then filtered through celite, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL, elution solvent: n-hexane:ethyl acetate=75:25 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 276 mg of the title compound (yield: 50%) as a colorless oil.

Mass spectrum (CI, m/z): 198 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.37-7.28 (m, 1H), 7.25-7.14 (m, 2H), 7.03-6.95 (m, 1H), 4.08 (dd, J=3.0, 10.5 Hz, 1H), 1.63 (dd, J=10.5, 13.9 Hz, 1H), 1.52 (dd, J=3.0, 13.9 Hz, 1H), 1.22 (s, 3H), 1.09 (s, 3H).

Reference Example 116 (R)-Ethyl 5-{[1-(3-fluorophenyl)-3-hydroxy-3-methylbutyl]carbamoyl}-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate

To a solution of 70 mg (0.35 mmol) of (R)-4-amino-4-(3-fluorophenyl)-2-methylbutan-2-ol synthesized in the similar manner as in Reference Example 115 in 5 ml of 1,4-dioxane, 0.31 ml (1.8 mol) of DIPEA and 172 mg (0.390 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 were added in this order with stirring at room temperature under argon stream and stirred at 90° C. for 2 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution allowed to cool to room temperature, followed by extraction from the mixed solution with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=70:30 to 27:73 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 149 mg of the title compound (yield: 70%) as a white foam.

Mass spectrum (CI, m/z): 602 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.78 (s, 1H), 7.36-7.26 (m, 1H), 7.19-7.12 (m, 2H), 7.01-6.93 (m, 1H), 6.71 (d, J=6.2 Hz, 1H), 4.96-4.88 (m, 1H), 4.67-4.60 (m, 2H), 4.54 (d, J=13.6 Hz, 1H), 4.41 (q, J=7.1 Hz, 2H), 2.59-2.42 (m, 2H), 2.29-2.21 (m, 2H), 2.02-1.84 (m, 3H), 1.66 (dd, J=3.2, 14.2 Hz, 1H), 1.59 (s, 3H), 1.54 (s, 3H), 1.33 (t, J=7.1 Hz, 3H), 1.14 (s, 3H), 1.13 (s, 3H), 0.11 (s, 9H).

Reference Example 117 (E)-Methyl 3-(2-fluorophenyl)acrylate

To a solution of 1.26 ml (12.1 mmol) of 2-fluorobenzaldehyde in 25 ml of dehydrated THF, 5.25 g (15.7 mmol) of methyl 2-(triphenylphosphoranylidene)acetate was added at room temperature under argon stream and then stirred for 17 hours with the temperature unchanged.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure. 20 ml of TBME was added to the obtained concentration residue, insoluble matter was filtered off, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 90:10 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 1.58 g of the title compound (yield: 73%) as a colorless oil.

Mass spectrum (CI, m/z): 181 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.83 (d, J=16.3 Hz, 1H), 7.57-7.50 (m, 1H), 7.40-7.33 (m, 1H), 7.20-7.07 (m, 2H), 6.55 (d, J=16.3 Hz, 1H), 3.82 (s, 3H).

Reference Example 118 (R)-Methyl 3-{benzyl[(S)-1-phenylethyl]amino}-3-(2-fluorophenyl)propanoate

To a solution of 2.94 ml (14.1 mmol) of (S)—N-benzyl-1-phenylethanamine in 30 ml of dehydrated THF, 8.22 ml (13.2 mmol) of a 1.6 M solution of n-butyllithium in n-hexane was added dropwise at −78° C. under argon stream and then stirred for 1 hour with the temperature unchanged. Subsequently, a solution of 1.58 g (8.77 mmol) of (E)-methyl 3-(2-fluorophenyl)acrylate synthesized in the similar manner as in Reference Example 117 in 5 ml of THF was added dropwise at −78° C. and then stirred for 1 hour with the temperature unchanged.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 1.27 g of the title compound (yield: 37%) as a pale yellow oil.

Mass spectrum (CI, m/z): 392 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.45-7.03 (m, 14H), 4.75 (dd, J=6.8, 8.9 Hz, 1H), 4.05 (q, J=6.9 Hz, 1H), 3.81 (d, J=14.6 Hz, 1H), 3.65 (d, J=14.6 Hz, 1H), 3.44 (s, 3H), 2.79 (dd, J=6.8, 14.9 Hz, 1H), 2.65 (dd, J=8.9, 14.9 Hz, 1H), 1.20 (d, J=6.9 Hz, 3H).

Reference Example 119 (R)-4-{Benzyl[(S)-1-phenylethyl]amino}-4-(2-fluorophenyl)-2-methylbutan-2-ol

To a solution of 1.27 g (3.24 mmol) of (R)-methyl 3-{benzyl[(S)-1-phenylethyl]amino}-3-(2-fluorophenyl)propanoate synthesized in the similar manner as in Reference Example 118 in 15 ml of dehydrated THF, 9.73 ml (9.73 mmol) of 1 M methyl magnesium bromide-THF solution was added dropwise at 0° C. under argon stream and then stirred at room temperature for 17 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction with ethyl acetate. The obtained organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, then filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=95:5 to 85:15 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 1.10 g of the title compound (yield: 87%) as a pale yellow oil.

Mass spectrum (CI, m/z): 392 [M+1]⁺.

¹H-NMR spectrum (400 MHz, CDCl₃) δ: 7.51-7.08 (m, 14H), 5.58 (s, 1H), 4.72 (dd, J=3.1, 11.3 Hz, 1H), 4.31 (d, J=12.9 Hz, 1H), 4.16-4.05 (m, 1H), 3.55 (d, J=12.9 Hz, 1H), 2.47 (dd, J=11.3, 14.6 Hz, 1H), 1.32 (dd, J=3.1, 14.6 Hz, 1H), 1.11 (s, 3H), 1.06 (d, J=7.0 Hz, 3H), 0.53 (s, 3H).

Reference Example 120 (R)-4-Amino-4-(2-fluorophenyl)-2-methylbutan-2-ol

To a solution of 1.1 g (2.8 mmol) of (R)-4-{benzyl[(S)-1-phenylethyl]amino}-4-(2-fluorophenyl)-2-methylbutan-2-ol synthesized in the similar manner as in Reference Example 119 in 10 ml of methanol, 200 mg of 20% palladium hydroxide/carbon (containing 50% water) was added at room temperature under argon stream and after replacement with a hydrogen atmosphere, stirred at room temperature for 6 hours. Subsequently, after replacement with an argon atmosphere, 354 mg (5.61 mmol) of ammonium formate was added at room temperature and stirred at 60° C. for 2 hours.

After the completion of the reaction, the reaction solution was diluted with ethyl acetate and then filtered through celite, and the filtrate was concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL, elution solvent: n-hexane:ethyl acetate=75:25 to 50:50 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 265 mg of the title compound (yield: 48%) as a colorless oil.

Mass spectrum (CI, m/z): 198 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.61-7.55 (m, 1H), 7.28-7.21 (m, 1H), 7.20-7.14 (m, 1H), 7.13-7.06 (m, 1H), 4.39 (dd, J=2.7, 10.4 Hz, 1H), 1.64 (dd, J=10.4, 13.8 Hz, 1H), 1.52 (dd, J=2.7, 13.8 Hz, 1H), 1.22 (s, 3H), 1.09 (s, 3H).

Reference Example 121 (R)-Ethyl 5-{[1-(2-fluorophenyl)-3-hydroxy-3-methylbutyl]carbamoyl}-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate

To a solution of 70 mg (0.35 mmol) of (R)-4-amino-4-(2-fluorophenyl)-2-methylbutan-2-ol synthesized in the similar manner as in Reference Example 120 in 5 ml of 1,4-dioxane, 0.309 ml (1.77 mol) of DIPEA and 235 mg (0.533 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 were added in this order with stirring at room temperature under argon stream and stirred at 90° C. for 2 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution allowed to cool to room temperature, followed by extraction from the mixed solution with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=65:35 to 29:71 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 150 mg of the title compound (yield: 70%) as a white solid.

Mass spectrum (CI, m/z): 602 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.79 (s, 1H), 7.54-7.46 (m, 1H), 7.27-7.07 (m, 3H), 6.70 (d, J=5.8 Hz, 1H), 5.24-5.16 (m, 1H), 4.71-4.54 (m, 3H), 4.42 (q, J=7.2 Hz, 2H), 2.58-2.44 (m, 2H), 2.32-2.22 (m, 2H), 2.02-1.87 (m, 3H), 1.67-1.57 (m, 4H), 1.53 (s, 3H), 1.34 (t, J=7.2 Hz, 3H), 1.19-1.14 (m, 6H), 0.13 (s, 9H).

Reference Example 122 (R)-Methyl 3-[(tert-butoxycarbonyl)amino]-4-methylpentanoate

To a solution of 600 mg (2.59 mmol) of (R)-3-[(tert-butoxycarbonyl)amino]-4-methylpentanoic acid in 6 ml of dichloromethane, 63 mg (0.52 mmol) of 4-dimethylaminopyridine and 0.53 ml (13 mmol) of methanol were added in this order with stirring at room temperature under argon stream.

Subsequently, 746 mg (3.89 mmol) of 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride was added in one portion with stirring at 0° C. and stirred at room temperature for 2 hours.

After the completion of the reaction, water was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate twice. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 80:20 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 630 mg of the title compound (yield: 99%) as a colorless oil.

Mass spectrum (CI, m/z): 246 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 6.72 & 6.37 (br d, J=9.2 Hz, total 1H), 3.71-3.61 (m, 1H), 3.60-3.52 (m, 3H), 2.44 (dd, J=4.6, 15.0 Hz, 1H), 2.30 (dd, J=9.4, 15.0 Hz, 1H), 1.71-1.58 (m, 1H), 1.36 (s, 9H), 0.86-0.73 (m, 6H).

Reference Example 123 (R)-tert-Butyl (5-hydroxy-2,5-dimethylhexan-3-yl)carbamate

To a solution of 630 mg (2.57 mmol) of (R)-methyl 3-[(tert-butoxycarbonyl)amino]-4-methylpentanoate synthesized in the similar manner as in Reference Example 122 in 6 ml of dehydrated THF, 7.7 ml (7.7 mol) of 1 M methyl magnesium bromide-THF solution was added dropwise with stirring at 0° C. under argon stream and stirred at room temperature for 4 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=91:9 to 70:30 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 133 mg of the title compound (yield: 21%) as a white solid.

Mass spectrum (CI, m/z): 246 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 6.53 & 6.14 (br d, J=8.9 Hz, total 1H), 4.09 (s, 1H), 3.47-3.39 (m, 1H), 1.63-1.50 (m, 1H), 1.42-1.33 (m, 11H), 1.06 (s, 3H), 1.05 (s, 3H), 0.80-0.74 (m, 6H).

Reference Example 124 (R)-4-Amino-2,5-dimethylhexan-2-ol hydrochloride

To a solution of 133 mg (0.542 mmol) of (R)-tert-butyl (5-hydroxy-2,5-dimethylhexan-3-yl)carbamate synthesized in the similar manner as in Reference Example 123 in 2 ml of 1,4-dioxane, 0.678 ml (2.71 mol) of 4 N hydrogen chloride/1,4-dioxane was added in one portion with stirring at room temperature under argon stream and stirred at room temperature for 3 hours. Subsequently, 0.678 ml (2.71 mol) of 4 N hydrogen chloride/1,4-dioxane was added in one portion with stirring at room temperature and stirred at room temperature for 15 hours.

After the completion of the reaction, the reaction solution was concentrated. 5 ml of n-hexane was added thereto and stirred at room temperature for 2 hours. The deposited solid was collected by filtration, washed with n-hexane, and dried under reduced pressure to obtain 58 mg of the title compound (yield: 59%) as a white solid.

Mass spectrum (CI, m/z): 146 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 8.25-4.63 (m, 3H), 3.16-3.04 (m, 1H), 1.96-1.82 (m, 1H), 1.58 (dd, J=2.0, 15.0 Hz, 1H), 1.49 (dd, J=9.8, 15.0 Hz, 1H), 1.21 (s, 3H), 1.17 (s, 3H), 0.91 (d, J=6.8 Hz, 3H), 0.89 (d, J=6.8 Hz, 3H).

Reference Example 125 (R)-Ethyl 5-[(5-hydroxy-2,5-dimethylhexan-3-yl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate

To a solution of 260 mg (0.590 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 in 4 ml of 1,4-dioxane, 0.342 ml (1.96 mol) of DIPEA and 57 mg (0.31 mmol) of (R)-4-amino-2,5-dimethylhexan-2-ol hydrochloride synthesized in the similar manner as in Reference Example 124 were added in this order with stirring at room temperature under argon stream and stirred at 90° C. for 1.5 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution allowed to cool to room temperature, followed by extraction from the mixed solution with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=70:30 to 30:70 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 99 mg of the title compound (yield: 57%) as a white foam.

Mass spectrum (CI, m/z): 550 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.78 (s, 1H), 5.83 (d, J=7.7 Hz, 1H), 4.55 (d, J=13.6 Hz, 1H), 4.47 (d, J=13.6 Hz, 1H), 4.42 (q, J=7.1 Hz, 2H), 4.30 (s, 1H), 3.73-3.62 (m, 1H), 2.58-2.43 (m, 2H), 2.31-2.21 (m, 2H), 1.96-1.82 (m, 2H), 1.75-1.57 (m, 8H), 1.50-1.42 (m, 1H), 1.34 (t, J=7.1 Hz, 3H), 1.10 (s, 3H), 1.08 (s, 3H), 0.89-0.78 (m, 6H), 0.15-0.08 (m, 9H).

Reference Example 126 Ethyl [1-(4-fluorophenyl)-2,2-dimethyl-3-oxopropyl]carbamate

To a solution of 2.63 g (29.5 mmol) of ethyl carbamate in 25 ml of toluene, 3.1 ml (29 mmol) of 4-fluorobenzaldehyde and 0.281 g (1.48 mmol) of p-toluenesulfonic acid monohydrate were added in this order with stirring at room temperature under argon stream and stirred at room temperature for 5 minutes. Subsequently, 2.68 ml (29.5 mmol) of isobutylaldehyde was added thereto dropwise with stirring at room temperature and stirred at 60° C. for 3 hours.

After the completion of the reaction, the reaction solution was poured to a saturated aqueous solution of sodium bicarbonate and subsequently stirred at room temperature for 5 minutes. An organic layer and an aqueous layer were separated, and then, the separated aqueous layer was subjected to extraction with toluene once. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, then dehydrated over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 69:31 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 3.85 g of the title compound (yield: 49%) as a colorless oil.

Mass spectrum (CI, m/z): 268 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.59 (s, 1H), 7.95 (d, J=10.1 Hz, 1H), 7.43-7.33 (m, 2H), 7.21-7.12 (m, 2H), 5.04 (d, J=10.1 Hz, 1H), 4.01-3.93 (m, 2H), 1.15 (t, J=7.1 Hz, 3H), 0.94 (s, 3H), 0.87 (s, 3H).

Reference Example 127 3-Amino-3-(4-fluorophenyl)-2,2-dimethylpropan-1-ol

To a solution of 3.84 g (14.4 mmol) of ethyl [1-(4-fluorophenyl)-2,2-dimethyl-3-oxopropyl]carbamate synthesized in the similar manner as in Reference Example 126 in 20 ml of ethanol, 0.326 g (8.62 mmol) of sodium borohydride was dividedly added with stirring at 0° C. under argon stream and stirred at room temperature for 1 hour. Subsequently, 1.61 g (28.7 mmol) of potassium hydroxide and water (10 ml) were added with stirring at room temperature and then stirred for 2 hours under heating to reflux.

After the completion of the reaction, the reaction solution allowed to cool was concentrated under reduced pressure, and ethanol was distilled off. The concentration residue was adjusted to pH 2 by adding 2 N hydrochloric acid and washed with diethyl ether. The aqueous layer was rendered basic (pH 9) by adding 1 N aqueous sodium hydroxide solution, followed by extraction with dichloromethane three times. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, then dehydrated over anhydrous sodium sulfate, filtered, concentrated under reduced pressure, and dried under reduced pressure to obtain 1.93 g of the title compound (yield: 68%) as a white solid.

Mass spectrum (CI, m/z): 198 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.38-7.29 (m, 2H), 7.15-7.03 (m, 2H), 3.81 (s, 1H), 3.25 (d, J=10.5 Hz, 1H), 3.13 (d, J=10.5 Hz, 1H), 0.74 (s, 3H), 0.65 (s, 3H).

Reference Example 128 Ethyl [1-(3-fluorophenyl)-2,2-dimethyl-3-oxopropyl]carbamate

To a solution of 2.63 g (29.5 mmol) of ethyl carbamate in 25 ml of toluene, 3.10 ml (29.5 mmol) of 3-fluorobenzaldehyde and 288 mg (1.51 mmol) of p-toluenesulfonic acid monohydrate were added in this order at room temperature in an argon atmosphere and then stirred at room temperature for 5 minutes. Subsequently, 2.70 ml (29.7 mmol) of isobutylaldehyde was added at room temperature and then stirred for 3 hours under heating to reflux after a Dean-Stark apparatus was loaded. Subsequently, 2.70 ml (29.7 mmol) of isobutylaldehyde was added and then further stirred for 3 hours under heating to reflux.

After the completion of the reaction, the reaction solution was poured to a saturated aqueous solution of sodium bicarbonate and then stirred at room temperature. After separation into an aqueous layer and an organic layer, the aqueous layer was subjected to extraction with toluene once. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 60:40 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 4.61 g of the title compound (yield: 59%) as a pale yellow oil.

Mass spectrum (CI, m/z): 268 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.59 (s, 1H), 7.95 (br d, J=10.2 Hz, 1H), 7.36 (dt, J=6.2, 7.9 Hz, 1H), 7.27-7.06 (m, 3H), 5.07 (d, J=10.2 Hz, 1H), 4.06-3.89 (m, 2H), 1.18-1.12 (m, 3H), 0.94 (s, 3H), 0.88 (s, 3H).

Reference Example 129 3-Amino-3-(3-fluorophenyl)-2,2-dimethylpropan-1-ol

To a solution of 4.75 g (17.8 mmol) of ethyl [1-(3-fluorophenyl)-2,2-dimethyl-3-oxopropyl]carbamate synthesized in the similar manner as in Reference Example 128 in 12 ml of ethanol, 352 mg (9.30 mmol) of sodium borohydride was dividedly added with stirring at 0° C. in an argon atmosphere and then stirred at room temperature for 4 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and 75 ml of dichloromethane was added to the residue. This solution was poured to 50 ml of a saturated aqueous solution of ammonium chloride, stirred at room temperature until foaming settled, and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with 25 ml of dichloromethane, all of the organic layers were dried over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=78:22 to 57:43 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure.

12 ml of ethanol and 2.45 g (37.1 mmol) of 85% potassium hydroxide were added to the obtained residue (3.91 g) and heated to reflux for 4 hours.

After standing to cool, the resultant was concentrated under reduced pressure, and 50 ml of water and 50 ml of dichloromethane were added thereto and stirred at room temperature. After separation into an aqueous layer and an organic layer, the aqueous layer was subjected to extraction with 50 ml of dichloromethane twice. All of the organic layers were dried over anhydrous sodium sulfate and then filtered, and the filtrate was concentrated under reduced pressure to obtain 2.58 g of the title compound (yield: 74%) as a pale yellow viscous liquid.

Mass spectrum (CI, m/z): 198 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.36-7.25 (m, 1H), 7.19-7.08 (m, 2H), 7.06-6.97 (m, 1H), 5.00 (br s, 1H), 3.81 (s, 1H), 3.25 (d, J=10.5 Hz, 1H), 3.14 (d, J=10.5 Hz, 1H), 1.99 (br s, 2H), 0.77 (s, 3H), 0.66 (s, 3H).

Reference Example 130 3-Amino-3-(2-fluorophenyl)-2,2-dimethylpropan-1-ol

To a solution of 2.62 g (29.4 mmol) of ethyl carbamate in 25 ml of toluene, 3.05 ml (29.2 mmol) of 2-fluorobenzaldehyde and 286 mg (1.51 mmol) of p-toluenesulfonic acid monohydrate were added in this order at room temperature in an argon atmosphere and then reacted at room temperature for 5 minutes. Subsequently, 2.70 ml (29.7 mmol) of isobutylaldehyde was added at 60° C. and then reacted at the same temperature as above for 5.5 hours.

After the completion of the reaction, the reaction solution was poured to a saturated aqueous solution of sodium bicarbonate and stirred at room temperature for 5 minutes. After separation into an aqueous layer and an organic layer, the aqueous layer was subjected to extraction with toluene once. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 60:40 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain a concentration residue.

To a solution of 6.23 g of the obtained residue in 15 ml of ethanol, 478 mg (12.6 mmol) of sodium borohydride was dividedly added with stirring at 0° C. in an argon atmosphere and then stirred at room temperature for 4 hours.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and 75 ml of dichloromethane was added to the residue. This solution was poured to 50 ml of a saturated aqueous solution of ammonium chloride, stirred at room temperature until foaming settled, and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with 25 ml of dichloromethane, all of the organic layers were dehydrated over anhydrous magnesium sulfate and filtered, and then, the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: n-hexane:ethyl acetate=77:23 to 56:44 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure.

15 ml of ethanol and 3.08 g (46.7 mmol) of 85% potassium hydroxide were added to 5.03 g of the obtained residue and heated to reflux for 5 hours.

After standing to cool, the resultant was concentrated under reduced pressure, 50 ml of water and 100 ml of dichloromethane were added, stirred at room temperature, and then the aqueous layer and the organic layer were separated. The aqueous layer was subjected to extraction with 50 ml of dichloromethane twice. Diethyl ether was added until the turbidity of all of the obtained organic layers was eliminated, then dried over anhydrous sodium sulfate, and filtered, and the filtrate was concentrated under reduced pressure to obtain 3.60 g of the title compound (yield: 63%) as a pale yellow viscous liquid.

Mass spectrum (CI, m/z): 198 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.55-7.49 (m, 1H), 7.30-7.21 (m, 1H), 7.20-7.13 (m, 1H), 7.12-7.03 (m, 1H), 5.03 (br s, 1H), 4.15 (s, 1H), 3.35 (d, J=10.5 Hz, 1H), 3.21 (d, J=10.5 Hz, 1H), 2.01 (br s, 2H), 0.73 (s, 3H), 0.71-0.66 (m, 3H).

Reference Example 131 Ethyl (2,2,4-trimethyl-1-oxopentan-3-yl)carbamate

To a solution of 2.06 g (23.1 mmol) of ethyl carbamate in 20 ml of toluene, 6.00 ml (66.1 mmol) of isobutylaldehyde and 224 mg (1.18 mmol) of p-toluenesulfonic acid monohydrate were added in this order at room temperature in an argon atmosphere and then stirred at room temperature for 5 minutes and at 60° C. for 4 hours.

After the completion of the reaction, the reaction solution was poured to a saturated aqueous solution of sodium bicarbonate and then stirred at room temperature. After separation into an aqueous layer and an organic layer, the aqueous layer was subjected to extraction with toluene once. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=90:10 to 60:40 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 1.55 g of the title compound (yield: 31%) as a pale yellow oil.

Mass spectrum (CI, m/z): 216 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.55 (s, 1H), 7.11 (br d, J=10.4 Hz, 1H), 4.01 (q, J=7.1 Hz, 2H), 3.67 (dd, J=6.2, 10.4 Hz, 1H), 1.80-1.66 (m, 1H), 1.17 (t, J=7.1 Hz, 3H), 0.98 (s, 3H), 0.90 (s, 3H), 0.80 (d, J=6.8 Hz, 3H), 0.75 (d, J=6.8 Hz, 3H).

Reference Example 132 3-Amino-2,2,4-trimethylpentan-1-ol

To a solution of 1.55 g (7.20 mmol) of ethyl (2,2,4-trimethyl-1-oxopentan-3-yl)carbamate synthesized in the similar manner as in Reference Example 131 in 10 ml of ethanol, 176 mg (4.66 mmol) of sodium borohydride was dividedly added at 0° C. in an argon atmosphere and then stirred at 0° C. for 1 hour and further at room temperature for 13.5 hours. Subsequently, 853 mg (15.2 mmol) of potassium hydroxide and 5.0 ml of water were added to the reaction solution at room temperature and then stirred for 3 hours under heating to reflux.

After the completion of the reaction, the reaction solution was concentrated under reduced pressure, and ethanol was distilled off. 2 N hydrochloric acid was added to the concentration residue and then washed with diethyl ether. After separation into an aqueous layer and an organic layer, the obtained the aqueous layer was adjusted to pH>10 by adding a 1 N aqueous sodium hydroxide solution, followed by extraction with dichloromethane three times. All of the obtained organic layers were washed with a saturated aqueous solution of sodium chloride, then dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (DIOL silica gel, elution solvent: 1,2-dichloroethane:n-hexane=30:70 to 100:0→1,2-dichloroethane:methanol=95:5 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 577 mg of the title compound (yield: 55%) as a colorless oil.

Mass spectrum (CI, m/z): 146 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 3.23 (d, J=10.4 Hz, 1H), 3.15 (d, J=10.4 Hz, 1H), 2.36 (d, J=1.8 Hz, 1H), 1.87 (dspt, J=1.8, 6.8 Hz, 1H), 0.88 (d, J=6.8 Hz, 3H), 0.81-0.76 (m, 9H).

Reference Example 133 (R)-Benzyl 2-butoxy-2-phenylacetate

To a suspension of 2.34 g (9.66 mmol) of (R)-benzyl 2-hydroxy-2-phenylacetate in 25.0 ml (219 mmol) of 1-iodobutane, 4.55 g (19.6 mmol) of silver(I) oxide was added at room temperature in an argon atmosphere and then reacted at 80° C. for 10.5 hours with stirring.

After the completion of the reaction, the reaction solution was allowed to cool to room temperature and then filtered using a celite filter. The filtration cake was washed with ethyl acetate, and then, all of the filtrates were concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=97:3 to 93:7 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure and dried under reduced pressure to obtain 1.65 g of the title compound (yield: 57%) as a colorless oil.

Mass spectrum (CI, m/z): 299 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.45-7.17 (m, 10H), 5.18-5.09 (m, 2H), 5.05 (s, 1H), 3.50 (td, J=6.4, 9.2 Hz, 1H), 3.40 (td, J=6.4, 9.2 Hz, 1H), 1.58-1.46 (m, 2H), 1.38-1.26 (m, 2H), 0.85 (t, J=7.4 Hz, 3H).

Reference Example 134 tert-Butyl (3-hydroxy-2,2-dimethyl-1-phenylpropyl)carbamate

To a solution of 1.00 g (5.58 mmol) of 3-amino-2,2-dimethyl-3-phenylpropan-1-ol [synthesized according to the method described in Synthetic Communications, 1994, 24 (7), 899-906] in 5 ml of dichloromethane, 2.34 ml (16.8 mmol) of triethylamine and 2.56 ml (11.1 mmol) of di-tert-butyl dicarbonate were added in this order at room temperature under argon stream and stirred at room temperature for 2 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution, followed by extraction from the mixed solution with ethyl acetate. The organic layer was washed with saturated saline, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=91:9 to 70:30 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 1.45 g of the title compound (yield: 93%) as a white solid.

Mass spectrum (CI, m/z): 280 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.37-7.18 (m, 6H), 4.97-4.75 (m, 1H), 4.62-4.32 (m, 1H), 3.22-3.08 (m, 1H), 3.05-2.90 (m, 1H), 1.40-1.29 (m, 9H), 0.83-0.73 (m, 6H).

Reference Example 135 tert-Butyl (3-methoxy-2,2-dimethyl-1-phenylpropyl)carbamate

To a solution of 600 mg (2.15 mmol) of tert-butyl (3-hydroxy-2,2-dimethyl-1-phenylpropyl)carbamate synthesized in the similar manner as in Reference Example 134 in 6 ml of dichloromethane, 370 mg (6.59 mmol) of potassium hydroxide was added in one portion with stirring at 0° C. under argon stream and stirred at 0° C. for 15 minutes. Subsequently, 0.407 ml (4.29 mmol) of dimethylsulfuric acid was added dropwise at 0° C. and stirred at room temperature for 8 hours.

After the completion of the reaction, water was added to the reaction solution, followed by extraction from the mixed solution with dichloromethane. The organic layer was washed with saturated saline, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=100:0 to 87:13 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 114 mg of the title compound (yield: 18%) as a colorless oil.

Mass spectrum (CI, m/z): 294 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.35-7.16 & 6.95-6.82 (m, total 6H), 4.67-4.37 (m, 1H), 3.28-3.19 (m, 3H), 3.08-2.91 (m, 1H), 2.88-2.76 (m, 1H), 1.43-1.13 (m, 9H), 0.90-0.82 (m, 3H), 0.81-0.70 (m, 3H).

Reference Example 136 3-Methoxy-2,2-dimethyl-1-phenylpropan-1-amine

To a solution of 114 mg (0.389 mmol) of tert-butyl (3-methoxy-2,2-dimethyl-1-phenylpropyl)carbamate synthesized in the similar manner as in Reference Example 135 in 2 ml of 1,4-dioxane, 0.486 ml (1.94 mmol) of 4 N hydrogen chloride/1,4-dioxane was added in one portion with stirring at room temperature under argon stream and stirred at room temperature for 20 hours.

After the completion of the reaction, the reaction solution was concentrated. The residue was dissolved by adding water and then adjusted to pH 8 by adding a saturated aqueous solution of sodium bicarbonate, followed by extraction with ethyl acetate twice. The organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to obtain 71 mg of the title compound (yield: 95%) as a colorless oil.

Mass spectrum (CI, m/z): 194 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 7.34-7.16 (m, 5H), 3.78 (s, 1H), 3.23 (s, 3H), 3.13 (d, J=8.8 Hz, 1H), 2.92 (d, J=8.8 Hz, 1H), 1.82 (br s, 2H), 0.83 (s, 3H), 0.70 (s, 3H).

Reference Example 137 Ethyl 5-[(3-methoxy-2,2-dimethyl-1-phenylpropyl)carbamoyl]-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate

To a solution of 70 mg (0.36 mmol) of 3-methoxy-2,2-dimethyl-1-phenylpropan-1-amine synthesized in the similar manner as in Reference Example 136 in 5 ml of 1,4-dioxane, 0.315 ml (1.81 mol) of DIPEA and 176 mg (0.399 mmol) of ethyl 5-(chlorocarbonyl)-6,6-dimethyl-3-[1-(trimethylsilyl)cyclobutanecarboxamido]-5,6-dihydropyrrolo[3,4-c]pyrazole-2(4H)-carboxylate synthesized in the similar manner as in Reference Example 3 were added in this order with stirring at room temperature under argon stream and stirred at 90° C. for 2 hours.

After the completion of the reaction, a saturated aqueous solution of ammonium chloride was added to the reaction solution allowed to cool to room temperature, followed by extraction from the mixed solution with ethyl acetate. The organic layer was washed with saturated saline, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The obtained concentration residue was subjected to silica gel column chromatography (elution solvent: n-hexane:ethyl acetate=61:39 to 40:60 (V/V)), and a fraction containing the compound of interest was concentrated under reduced pressure to obtain 131 mg of the title compound (yield: 61%) as a white foam.

Mass spectrum (CI, m/z): 598 [M+1]⁺.

¹H-NMR spectrum (400 MHz, DMSO-d₆) δ: 9.75 (s, 1H), 7.38-7.20 (m, 5H), 6.78 (d, J=8.3 Hz, 1H), 4.64-4.50 (m, 3H), 4.42 (q, J=7.1 Hz, 2H), 3.40 (s, 3H), 3.15 (d, J=9.2 Hz, 1H), 2.93 (d, J=9.2 Hz, 1H), 2.57-2.45 (m, 2H), 2.32-2.23 (m, 2H), 1.97-1.82 (m, 2H), 1.61 (s, 3H), 1.52 (s, 3H), 1.35 (t, J=7.0 Hz, 3H), 1.13 (s, 3H), 0.68 (s, 3H), 0.13 (s, 9H).

Test Example 1

CDK7 Enzyme Inhibition Test

The preparation of a buffer solution was performed by mixing a N-2-hydroxyethylpiperazine-N′-2-ethanesulfonic acid buffer solution (HEPES buffer solution) (pH 7.4), dithiothreitol (DTT), Triton X-100, and magnesium chloride (MgCl₂). A 500 μM [γ-³³P]ATP solution was used by diluting a 10 mM ATP solution and a commercially available [γ-³³P]ATP solution (manufactured by PerkinElmer, Inc., Code No. NEG-302H) with the buffer solution. A CDK7 solution was used by diluting commercially available CDK7 (manufactured by Carna Biosciences, Inc., Catalog No. 04-108) with the buffer solution. A substrate solution was used by diluting myelin basic protein (MBP) with the buffer solution. As for the preparation of a reaction solution, the buffer solution, the 500 μM [γ-³³P]ATP solution, the CDK7 solution, and the substrate solution were mixed at 4° C. to obtain a reaction solution.

CDK7 enzyme reaction was performed by adding 5 μL of a test compound solution prepared with 10% dimethyl sulfoxide (DMSO)/90% injectable distilled water, and 45 μL of the reaction solution to a 1.5 mL microtube at 4° C. and reacting in the microtube at 30° C. for 20 minutes in a water bath incubator. After the reaction, a 10% aqueous trichloroacetic acid (TCA) solution was added to each microtube while cooled to 4° C., and mixed to terminate the reaction. The resultant was left standing at 4° C. for 10 minutes and then centrifuged in a centrifuge, and the supernatant was discarded. Next, a 2% aqueous TCA solution was added, mixed, and then centrifuged in a centrifuge, and the supernatant was discarded. This washing operation was performed twice. After the washing, precipitates were dissolved in a 1 N aqueous sodium hydroxide (NaOH) solution, and the energy quantity (radioactivity) of the reaction product was measured with a liquid scintillation counter.

The calculation of the inhibitory activity of the test compound against CDK7 was performed as a test compound concentration inhibiting 50% of the amount of ³³P bound to MBP (IC₅₀ value) by using EXSUS (version 8.0.0 or version 8.0.1, manufactured by CAC Exicare Corp.).

The calculation of a Ki value was performed according to the following calculation expression. S means the concentration of ATP contained in the reaction solution, and Km means a Michaelis-Menten constant. Ki=IC ₅₀/(1+S/Km)

In this test, the compounds of the present invention exhibited excellent CDK7 inhibitory activity, and, for example, the Ki values of compound Nos. II-114, II-116, III-114, III-170, III-226, III-298, III-353, 111-592, III-1059, III-1140, IV-2, IV-114, IV-117, IV-119, IV-123, IV-139, IV-171, IV-227, IV-283, IV-291, IV-299, IV-362, IV-378, IV-403 (sodium salt), IV-438, IV-442, IV-446, IV-450, IV-455, IV-475, IV-495, IV-510, IV-519, IV-527, IV-534, IV-542, IV-632, IV-633, IV-634, IV-673, IV-743, IV-786, IV-787, IV-815, IV-822, IV-862, IV-911, IV-920, IV-939, IV-959, IV-1067, IV-1175, IV-1176, IV-1178, IV-1180, IV-1188, IV-1196, IV-1204, IV-1208, IV-1215, IV-1241, IV-1255, IV-1258, IV-1274, IV-1330, IV-1348, IV-1372, IV-1383, IV-1404, IV-1427, IV-1546, and IV-1547 were 50 nM or lower.

Test Example 2

CDK2 Enzyme Inhibition Test

The preparation of a buffer solution was performed by mixing a HEPES buffer solution (pH 7.4), DTT, Triton X-100, and MgCl₂. A 500 μM [γ-³³P]ATP solution was used by diluting a 10 mM ATP solution and a commercially available [γ-³³P]ATP solution (manufactured by PerkinElmer, Inc., Code No. NEG-302H) with the buffer solution. A CDK2 solution was used by diluting commercially available CDK2 (manufactured by Invitrogen Corp., Catalog No. PV3267) with the buffer solution. A substrate solution was used by diluting MBP with the buffer solution. As for the preparation of a reaction solution, the buffer solution, the 500 μM [γ-³³P]ATP solution, the CDK2 solution, and the substrate solution were mixed at 4° C. to obtain a reaction solution.

CDK2 enzyme reaction was performed by adding 5 μL of a test compound solution prepared with 10% DMSO/90% injectable distilled water, and 45 μL of the reaction solution in a 1.5 mL microtube at 4° C. and reacting in the microtube at 30° C. for 20 minutes in a water bath incubator. After the reaction, a 10% aqueous TCA solution was added to each microtube while cooled to 4° C., and mixed to terminate the reaction. The resultant was left standing at 4° C. for 10 minutes and then centrifuged in a centrifuge, and the supernatant was discarded. Next, a 2% aqueous TCA solution was added, mixed thereto, and then centrifuged in a centrifuge, and the supernatant was discarded. This washing operation was performed twice. After the washing, precipitates were dissolved in a 1 N aqueous NaOH solution, and the radioactivity was measured with a liquid scintillation counter.

The calculation of the inhibitory activity of the test compound against CDK2 was performed as a test compound concentration inhibiting 50% of the amount of ³³P bound to MBP (IC₅₀ value) by using EXSUS (version 8.0.0 or version 8.0.1, manufactured by CAC Exicare Corp.).

The calculation of a Ki value was performed according to the following calculation expression. S means the concentration of ATP contained in the reaction solution, and Km means a Michaelis-Menten constant. Ki=IC ₅₀/(1+S/Km)

In this test, the Ki values of CDK2 inhibitory activity of the compounds of the present invention, for example, compound Nos. II-114, II-116, III-114, III-298, III-353, IV-2, IV-114, IV-115, IV-117, IV-119, IV-123, IV-171, IV-227, IV-283, IV-291, IV-299, IV-403 (sodium salt), IV-438, IV-442, IV-450, IV-455, IV-475, IV-495, IV-534, IV-632, IV-718, IV-743, IV-822, IV-883, IV-890, IV-911, IV-939, IV-946, IV-1184, IV-1196, IV-1204, and IV-1258 were 1000 nM or higher; thus they had high selectivity for CDK7 inhibitory activity with respect to CDK2 inhibitory activity.

Test Example 3

PAK4 Enzyme Inhibition Test

The preparation of a buffer solution was performed by mixing a trishydroxyaminomethane buffer solution (Tris buffer solution) (pH 7.5), DTT, Triton X-100, MgCl₂, ethylene glycol bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid (EGTA), β-glycerol phosphate, and sodium orthovanadate(V). A 40 μM [γ-³³P]ATP solution was used by diluting a 10 mM ATP solution and a commercially available [γ-³³P]ATP solution (manufactured by PerkinElmer, Inc., Code No. NEG-302H) with the buffer solution. A PAK4 solution was used by diluting commercially available PAK4 (manufactured by Invitrogen Corp., Catalog No. PV4212) with the buffer solution. A substrate solution was used by diluting MBP with the buffer solution. As for the preparation of a reaction solution, the buffer solution, the 40 μM [γ-³³P]ATP solution, the PAK4 solution, and the substrate solution were mixed at 4° C. to obtain a reaction solution.

PAK4 enzyme reaction was performed by adding 5 μL of a test compound solution prepared with 10% DMSO/90% injectable distilled water, and 45 IpL of the reaction solution in a 1.5 mL microtube at 4° C. and reacting in the microtube at 30° C. for 20 minutes in a water bath incubator. After the reaction, a 10% aqueous TCA solution was added to each microtube while cooled to 4° C., and mixed to terminate the reaction. The resultant was left standing at 4° C. for 10 minutes and then centrifuged in a centrifuge, and the supernatant was discarded. Next, a 2% aqueous TCA solution was added, mixed, and then centrifuged in a centrifuge, and the supernatant was discarded. This washing operation was performed twice. After the washing, precipitates were dissolved in a 1 N aqueous NaOH solution, and the radioactivity was measured with a liquid scintillation counter.

The calculation of the inhibitory activity of the test compound against PAK4 was performed as a test compound concentration inhibiting 50% of the amount of ³³P bound to MBP (IC₅₀ value) by using EXSUS (version 8.0.0 or version 8.0.1, manufactured by CAC Exicare Corp.).

The calculation of a Ki value was performed according to the following calculation expression. S means the concentration of ATP contained in the reaction solution, and Km means a Michaelis-Menten constant. Ki=IC ₅₀/(1+S/Km)

In this test, the Ki values of PAK4 inhibitory activity of the compounds of the present invention, for example, compound Nos. II-114, II-116, III-114, III-298, III-353, IV-2, IV-114, IV-115, IV-117, IV-119, IV-123, IV-171, IV-227, IV-283, IV-291, IV-299, IV-403 (sodium salt), IV-438, IV-442, IV-450, IV-455, IV-475, IV-495, IV-534, IV-632, IV-673, IV-718, IV-743, IV-822, IV-883, IV-911, IV-918, IV-946, IV-1184, IV-1204, IV-1208, IV-1258, IV-1383, IV-1404, and IV-1546 were 500 nM or higher; thus they had high selectivity for CDK7 inhibitory activity with respect to PAK4 inhibitory activity.

Test Example 4

Human Large Intestine Cancer (HCT-116) Cell Growth Inhibition Test

The measurement of a human large intestine cancer cell growth inhibitory effect was carried out by modifying the method of Simak et al. (Cancer Research, 69, 6208 (2009)).

A human large intestine cancer cell line (HCT-116) (manufactured by DS Pharma Biomedical Co., Ltd., Cat. No. EC91091005) was cultured in McCoy's 5a (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 16600-082) medium containing 10% FBS (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 10082-147) and 1% penicillin/streptomycin/amphotericin B (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 15240-096) and inoculated at 1.0×10³ cells/well in a 96-well plate (manufactured by Corning Inc., REF. 353072). After overnight culture in a carbon dioxide incubator, it was replaced with a fresh McCoy's 5a medium containing 10% FBS on the next day, and a test compound dissolved in DMSO (manufactured by Wako Pure Chemical Industries, Ltd., Code No. 043-07216) (final DMSO concentration: 0.1%) was added and left standing in a carbon dioxide incubator. After culturing for 3 days, the absorbance of each well was measured by using In Vitro Toxicology Assay Kit Sulforhodamine B based (manufactured by Sigma-Aldrich Co. LLC., Pcode 1001910706).

The rate of inhibition of cell growth at each concentration was calculated from the test compound concentration and the absorbance of sulforhodamine B, and the concentration of the test compound necessary for inhibiting 50% of cell growth (IC₅₀ value) was calculated by using EXSUS (version 8.0.0 or version 8.0.1, manufactured by CAC Exicare Corp.).

In this test, the compounds of the present invention exhibited excellent HCT-116 cell growth inhibitory activity, and, for example, the IC₅₀ values of compound Nos. II-114, II-116, III-114, III-170, III-226, III-298, III-353, III-592, III-1059, III-1140, IV-2, IV-114, IV-117, IV-119, IV-123, IV-131, IV-139, IV-171, IV-227, IV-235, IV-283, IV-291, IV-299, IV-354, IV-362, IV-378, IV-438, IV-442, IV-446, IV-450, IV-475, IV-495, IV-510, IV-519, IV-527, IV-534, IV-558, IV-562, IV-632, IV-633, IV-634, IV-672, IV-673, IV-718, IV-743, IV-759, IV-786, IV-787, IV-815, IV-822, IV-861, IV-862, IV-883, IV-890, IV-911, IV-918, IV-939, IV-946, IV-959, IV-1067, IV-1175, IV-1176, IV-1178, IV-1180, IV-1184, IV-1188, IV-1196, IV-1204, IV-1208, IV-1211, IV-1215, IV-1224, IV-1241, IV-1255, IV-1258, IV-1266, IV-1268, IV-1274, IV-1330, IV-1348, IV-1383, IV-1404, IV-1427, and IV-1546 were 500 nM or lower.

Test Example 5

Human Breast Cancer(MCF-7) Cell Growth Inhibition Test

The measurement of a human breast cancer cell growth inhibitory effect was carried out by modifying the method of Simak et al. (Cancer Research, 69, 6208 (2009)).

A human breast cancer cell line (MCF-7) manufactured by DS Pharma Biomedical Co., Ltd., Cat. No. EC86012803, was cultured in MEM (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 11095-080) medium containing 10% FBS (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 10082-147), nonessential amino acids (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 11140-050), and 1% penicillin/streptomycin/amphotericin B (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 15240-096) and inoculated at 3.0×10³ cells/well to a 96-well plate (manufactured by Corning Inc., REF. 353072). After overnight culture in a carbon dioxide incubator, it was replaced with a fresh MEM medium containing 10% FBS, nonessential amino acids, and 1% penicillin/streptomycin/amphotericin B on the next day, and a test compound dissolved in DMSO (manufactured by Wako Pure Chemical Industries, Ltd., Code No. 043-07216) (final DMSO concentration: 0.1%) was added and left standing in a carbon dioxide incubator. After culture for 3 days, the absorbance of each well was measured by using In Vitro Toxicology Assay Kit Sulforhodamine B based (manufactured by Sigma-Aldrich Co. LLC., Pcode 1001910706).

The rate of inhibition of cell growth at each concentration was calculated from the test compound concentration and the absorbance of sulforhodamine B, and the concentration of the test compound necessary for inhibiting 50% of cell growth (IC₅₀ value) was calculated by using EXSUS (version 8.0.0 or version 8.0.1, manufactured by CAC Exicare Corp.).

In this test, the compounds of the present invention exhibited excellent MCF-7 cell growth inhibitory activity, and, for example, the IC₅₀ values of compound Nos. IV-114, IV-117, IV-123, IV-171, IV-227, IV-291, IV-438, IV-455, IV-475, and IV-495 were 500 nM or lower.

Test Example 6

Human Peripheral Blood Mononuclear Cell (PBMC) CD3/CD28-Induced IL-2 Production Inhibition Test

PBMC was separated and collected by using Ficoll-Paque (17-1440-02 manufactured by GE Healthcare Japan Corp.) from blood collected from healthy human adult in the presence of heparin. RPMI1640 medium (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 11875) containing 10% FBS (manufactured by GIBCO/Thermo Fisher Scientific, Inc. REF. 10082) and containing a test compound dissolved in DMSO and 2 μg/mL anti-hCD28 (manufactured by R&D Systems, Inc., Cat. No. MAB342) was added at 100 μL/well to T cell Activation Plate Anti-Human CD3 96-well plate (manufactured by Corning Inc., REF. 354725), and subsequently, a PBMC suspension adjusted such that the number of cells was 2×10⁶ cells/mL was added at 100 μL/well (final DMSO concentration: 0.1%). A RPMI1640 medium containing 10% FBS and containing 0.1% DMSO and 2 μg/mL anti-hCD28 was similarly added to wells not supplemented with the test compound. After incubation for 2 days in a carbon dioxide incubator, the culture supernatant was collected. The collected culture supernatant was stored at −20° C. until IL-2 content measurement.

In the measurement of IL-2 content in the culture supernatant, a sandwich ELISA kit Quantikine Human IL-2 (manufactured by R&D Systems, Inc., Cat. No. S2050) was used. The IL-2 content of each sample was calculated from the calibration curve of Standard IL-2 included in the kit. When the amount of IL-2 produced by CD3/CD28 stimulation in the case of the addition of only DMSO was defined as 100%, the rate of inhibition of IL-2 production at each concentration of the test compound was calculated. A test compound concentration inhibiting 50% of IL-2 production was calculated as an IC₅₀ value (nM) from the concentration of the added test compound and the rate of inhibition of IL-2 production by the test compound by using EXSUS (version 8.0.0 or version 8.0.1, manufactured by CAC Exicare Corp.).

In this test, the compounds of the present invention exhibited excellent IL-2 production inhibitory activity, and, for example, the IC₅₀ values of compound Nos. II-114, III-114, III-170, III-226, IV-114, IV-123, IV-139, IV-171, IV-227, IV-235, IV-283, IV-299, IV-354, IV-450, IV-510, IV-519, IV-527, IV-1175, IV-1178, IV-1180, IV-1188, and IV-1255 were 50 nM or lower.

Test Example 7

Human PBMC Various-Stimulant Cocktail-Induced IL-17 Production Inhibition Test

PBMC was separated and collected by using Ficoll-Paque (17-1440-02 manufactured by GE Healthcare Japan Corp.) from blood collected from healthy human adult in the presence of heparin. The collected PBMC was further cultured in a flask for a certain time, and then, non-adherent cells in the supernatant were collected and used as a T-cell suspension. RPMI1640 medium (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 11875), which is containing 10% FBS (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 10082), 1% penicillin/streptomycin/amphotericin B (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 15240-096), 1% nonessential amino acids (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 11140-050), and 1% pyruvic acid (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 11140) and containing a test compound dissolved in DMSO, 2 μg/mL (final concentration) CD28 antibody (manufactured by BioLegend, Inc., Cat. No. 302914), 10 μg/mL (final concentration) human IFN-γ antibody (manufactured by BD Biosciences, Cat. No. 554698), 10 μg/mL (final concentration) human IL-4 antibody (manufactured by BD Biosciences, Cat. No. 554481), 20 ng/mL (final concentration) human IL-6 (manufactured by BioLegend, Inc., Cat. No. 570802), 10 ng/mL (final concentration) human IL-23 (manufactured by BioLegend, Inc., Cat. No. 574102), 10 ng/mL (final concentration) human IL-113 (manufactured by PeproTech Inc., Cat. No. 200-01B), and 10 ng/mL (final concentration) human TGF-β (manufactured by BioLegend, Inc., Cat. No. 580702), was added at 100 μL/well to T cell Activation Plate Anti-Human CD3 96-well plate (manufactured by Corning Inc., REF. 354725). Subsequently, 100 μL of a T-cell suspension adjusted to 2×10⁵ cells/mL was added to each well (final DMSO concentration: 0.1%). Only DMSO was added to wells in the absence of the test compound. After incubation for 5 days in a carbon dioxide incubator, the culture supernatant was collected and stored at −20° C. until IL-17 content measurement.

In the IL-17 content measurement in the culture supernatant, a sandwich ELISA kit (Quantikine Human IL-17, manufactured by R&D Systems, Inc.) was used. The IL-17 content of each sample was calculated from the calibration curve of Standard IL-17 included in the kit. When the amount of IL-17 produced by the cocktail of various stimulants in the case of the addition of only DMSO was defined as 100%, the rate of inhibition of IL-17 production at each concentration of the test compound was calculated. The concentration of the test compound necessary for inhibiting 50% of IL-17 production (IC₅₀ value) was calculated from the concentration of the added test compound and the rate of inhibition of IL-17 production by the test compound by using EXSUS (version 8.0.0 or version 8.0.1, manufactured by CAC Exicare Corp.).

In this test, the compounds of the present invention exhibited excellent IL-17 production inhibitory activity, and, for example, the IC₅₀ values of compound Nos. IV-299, IV-354, IV-673, IV-718, IV-743, IV-911, IV-918, IV-939, IV-946, IV-1175, IV-1178, IV-1180, IV-1184, IV-1188, IV-1196, IV-1204, IV-1208, IV-1383, IV-1404, and IV-1546 were 50 nM or lower.

Test Example 8

Human Keratinocyte Growth Inhibition Assay

The measurement of a human keratinocyte growth inhibitory effect was carried out by modifying the method of Schafer et al. (British Journal of Pharmacology, 159, 842 (2011)).

Human keratinocytes (NHEK-Neo Pooled, manufactured by Lonza Group AG, Cat. No. 00192906) were cultured in KGM-Gold Bullet Kit (manufactured by Lonza Group AG, Cat. No. 00192060) and inoculated at 2.0×10³ cells/well to a 96-well plate. After overnight culture in a carbon dioxide incubator, a test compound dissolved in DMSO (final DMSO concentration: 0.1%) was added and left standing in a carbon dioxide incubator. After culture for 2 days, the absorbance thereof was measured by using Cell Counting Kit-8 (343-07623 manufactured by Dojindo Laboratories)).

The rate of inhibition of cell growth at each concentration was calculated from the test compound concentration and the absorbance of Cell Counting Kit-8, and the concentration of the test compound necessary for inhibiting 50% of cell growth (IC₅₀ value) was calculated by using EXSUS (version 8.0.0 or version 8.0.1, manufactured by CAC Exicare Corp.).

In this test, the compounds of the present invention exhibited excellent human keratinocyte growth inhibitory activity, and, for example, the IC₅₀ values of compound Nos. III-170, III-226, III-1059, IV-123, IV-131, IV-139, IV-171, IV-227, IV-235, IV-299, IV-354, IV-378, IV-519, IV-527, IV-1175, IV-1178, IV-1180, and IV-1188 were 500 nM or lower.

Test Example 9

IL-6 Production Inhibition Test in Rat Adjuvant Arthritis Model

A single-dose drug efficacy test using rat adjuvant arthritis models was carried out by modifying the method of Magari. K et al. (J. Rheumatol. 30 (10), 2193 (2003)).

LEW rats (female, supplied by Charles River Laboratories Japan, Inc.) were used as laboratory animals. An adjuvant prepared from heat-killed bacteria of Mycobacterium butyricum (264010 manufactured by Difco Laboratories Ltd.) and liquid paraffin (manufactured by Wako Pure Chemical Industries, Ltd., Code No. 128-04375) was subcutaneously administered as a phlogogenic material to the right hind leg footpads of the rats under inhalation anesthesia with isoflurane (manufactured by Wako Pure Chemical Industries, Ltd., Code No. 099-06571) to prepare arthritis models. Approximately 2 weeks later, left paw edema was measured with a paw volume meter (model TK-101CMP manufactured by Unicom Co., Ltd.), and grouping was performed such that the average volume of left paw edema was equal among groups. A test compound or only a solvent was administered, after a certain time, they were sacrificed by exsanguination from the abdomens under isoflurane anesthesia, and the left ankles were collected, chopped, and frozen by using liquid nitrogen. The collected left ankle portions were disrupted in CRYOPress (model CP-100WP manufactured by Microtec Co., Ltd.), then supplemented with a buffer solution, shaken overnight at 4° C., and then centrifuged to collected a supernatant. The preparation of the buffer solution was performed by mixing a Tris buffer solution (pH 7.4), sodium chloride (NaCl), phenyl methyl sulfonyl fluoride (PMSF), Triton X-100, EDTA-free complete tablets (manufactured by F. Hoffmann-La Roche, Ltd., REF. 11 873 580 001), and Otsuka distilled water (manufactured by Otsuka Pharmaceutical Co., Ltd., product No. 1323). IL-6 in the collected supernatant was measured by using a sandwich ELISA kit (manufactured by R&D Systems, Inc., Catalog No. S6050).

The IL-6 content of each sample was calculated from the calibration curve of Standard IL-6 included in the kit. When the amount of IL-6 produced in the solvent administration control group was defined as 100%, the rate of inhibition of IL-6 production (%) at each dose of the test compound was calculated.

In this test, the compounds of the present invention exhibited excellent IL-6 production inhibitory activity, and, for example, compound Nos. II-114, IV-2, IV-119, IV-171, and IV-235 exhibited 50% or more rate of inhibition by the administration of 10 mg/kg, and compound Nos. IV-123, IV-139, IV-227, IV-299, and IV-632 exhibited 50% or more rate of inhibition by the administration of 3 mg/kg.

Test Example 10

Paw Edema Suppression Test in Rat Adjuvant Arthritis Model

LEW rats (female, supplied by Charles River Laboratories Japan, Inc.) were used as laboratory animals. An adjuvant prepared from heat-killed bacteria of Mycobacterium butyricum (264010 manufactured by Difco Laboratories Ltd.) and liquid paraffin (manufactured by Wako Pure Chemical Industries, Ltd., Code No. 128-04375) was subcutaneously administered as a phlogogenic material to the right hind leg footpads of the rats under inhalation anesthesia with isoflurane (manufactured by Wako Pure Chemical Industries, Ltd., Code No. 099-06571) to prepare arthritis models. Also, liquid paraffin not containing the killed bacteria was administered by a similar method to obtain an untreated group. The administration of the test compound or only the solvent was performed by oral administration 28 times once a day from the adjuvant injection day (day 0) to day 27. The volumes of the adjuvant-administered right hind legs and the non-administered left hind legs were measured several times on days 7 to 28 after the adjuvant administration with a paw volume meter (model TK-101CMP manufactured by Unicom Co., Ltd.), and the rate of edema was calculated according to the following expression. Rate of edema (%)=[{(Footpad volume at the time of measurement)−(Footpad volume before the start of the test)}/(Footpad volume before the start of the test)]×100

The rate of suppression of edema in the solvent-administered control group was further calculated according to the following expression. Rate of suppression of edema (%)=[1−{(Rate of edema of the test compound-administered group)−(Rate of edema of the untreated group)}/{Rate of edema of the control group)−(Rate of edema of the untreated group)}]×100

In this test, the compounds of the present invention exhibited excellent edema suppressive activity, and, for example, compound Nos. IV-114 and IV-171 exhibited 50% or more rate of suppression by the administration of 10 mg/kg.

Test Example 11

Tumor Growth Inhibition Test in Human Large Intestine Cancer Cell (HCT 116)-Subcutaneously Transplanted Nude Mouse

A human large intestine cancer cell line (HCT-116) (manufactured by DS Pharma Biomedical Co., Ltd., Cat. No. EC91091005) was cultured in a McCoy's 5a medium containing 10% FBS (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 10082-147) and 1% penicillin/streptomycin/amphotericin B (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF.15240-096) and adjusted to 1.0×10⁸ cells/mL with PBS (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 10010-031) or Hanks solution (HBSS(−)) (manufactured by GIBCO/Thermo Fisher Scientific, Inc., REF. 14025-076). The adjusted cell suspension was subcutaneously injected at 0.1 mL/mouse to the right abdomens of BALB/c-nu/nu mice (female, supplied by Charles River Laboratories Japan, Inc.). After rearing for a certain period, the long diameter (mm) and short diameter (mm) of tumor were measured with electronic calipers (manufactured by Mitsutoyo Corp., Cat. 500-712-10), and the tumor volume was calculated according to the following expression. Tumor volume (mm³)=(Long diameter)×(Short diameter)×(Short diameter)×0.5

Individuals whose tumor volume was within the range of 50 to 200 mm³ were selected and grouped such that the tumor volume was almost equivalent, and then, a test compound or only a solvent was orally administered. When the first day of administration was defined as day 0, the oral administration was repeated once a day up to day 3, and the tumor size was measured on day 4. When increase in tumor volume from day 0 of the solvent-administered control group was defined as 100%, the rate of suppression of tumor volume (%) at each dose of the test compound was calculated.

In this test, the compounds of the present invention exhibited excellent tumor growth inhibitory activity, and, for example, compound Nos. III-170, IV-171, IV-299, and IV-632 exhibited 50% or more rate of inhibition by the administration of 100 mg/kg.

Test Example 12

Ear Thickening Suppression Test Using Mouse Imiquimod-Induced Psoriasis Model

An imiquimod-induced psoriasis model test was carried out by modifying the method of Leslie van der Fits et al. (J. Immunol. 182, 5836 (2009)). BALB/c mice were used (female, supplied by Charles River Laboratories Japan, Inc.) as laboratory animals. On the start day of the test, the thicknesses of the right auricles of the mice were measured with a thickness gauge (model SMD-565J manufactured by TECLOCK Corp.). A test compound solution or only a solvent was applied or orally administered, and after 60 minutes, 5 mg of imiquimod (Beselna Cream 5% manufactured by Mochida Pharmaceutical Co., Ltd.) was applied to the insides of the right auricles. The test compound solution or solvent administration and the imiquimod application were carried out for 4 days, and the thicknesses of the right auricles were measured again on day 5. When increase in the thicknesses of the right auricles of the solvent-administered group on day 5 was defined as 100%, the rate of inhibition of increase (%) at each dose of the test compound was calculated.

In this test, the compounds of the present invention exhibited excellent activity, and, for example, compound Nos. IV-114, IV-123, IV-227, V-1442, V-1446, V-1454, V-1462, V-1470, and V-1474 exhibited 50% or more rate of inhibition by the application of a 1% solution in methanol, and compound Nos. III-1059, IV-299, IV-354, IV-673, IV-676, IV-718, IV-743, IV-911, IV-918, IV-939, IV-946, IV-1175, IV-1178, IV-1180, IV-1184, IV-1188, IV-1196, IV-1200, IV-1204, IV-1208, IV-1383, IV-1404, and IV-1546 exhibited 50% or more rate of inhibition by the application of a 0.01% methanol solution.

Test Example 13

Metabolism Test Using Human Liver Microsome Fraction

To a reaction composition solution (50 μL of NADPH production system solution A (manufactured by Corning Inc., REF. 451220), 10 μL of NADPH production system solution B (manufactured by Corning Inc., REF. 451200), 40 μL of 250 mM UDP-glucuronic acid, 200 μL of UGT Reaction Mix solution B (manufactured by Corning Inc., REF. 451320), and 590 μL of distilled water) in which human liver microsome (manufactured by Sekisui XenoTech, LLC., Cat No. H610) corresponding to 2 mg of protein was suspended, 10 μL of a test compound (prodrug represented by formula (V) or (VI)) dissolved in DMSO (manufactured by Wako Pure Chemical Industries, Ltd., Code No. 043-07216) (final DMSO concentration: 1.0%) was added and incubated at 37° C. for 5 minutes.

The peak areas (measurement UV wavelength: 245 nm) of the test compound (prodrug represented by formula (V) or (VI)) and an alcohol form which was a produced pharmacologically active form were calculated by high-performance liquid chromatography (model LC-20A series manufactured by Shimadzu Corp.).

HPLC conditions: column: Phenomenex Kinetex C18 (manufactured by Phenomenex Inc., Part No. 00D-4462-AN), 2.1 mm×100 mm, 2.6 μm, column temperature: 40° C., eluent: solution A: 0.1% formic acid (manufactured by Wako Pure Chemical Industries, Ltd., Code No. 063-04192), solution B: acetonitrile (manufactured by Wako Pure Chemical Industries, Ltd., Code No. 019-08631)/methanol (manufactured by Wako Pure Chemical Industries, Ltd., Code No. 138-06473)/formic acid=500/500/1, gradient conditions: 0→3 min: 90% solution A, 3→11 min: 20% solution A→5%, 11→15 min: 5% solution A, analysis time: 20 min)

In this test, for example, for compound No. V-1442, only the peak of compound No. IV-114 which was a produced alcohol form was detected after incubation for 5 minutes.

In this test, the prodrug of the present invention was immediately converted to the pharmacologically active form.

From the results of Test Examples 1 to 13 described above, it is concluded that the compound of the present invention has excellent CDK7 inhibitory activity and high selectivity in itself or functions as a prodrug of a compound having excellent CDK7 inhibitory activity and high selectivity, and is useful as, for example, a therapeutic drug and/or a prophylactic drug for cancers or inflammatory diseases.

A novel substituted dihydropyrrolopyrazole compound having a particular structure represented by formula (I) of the present invention or a pharmacologically acceptable salt thereof has excellent CDK7 inhibitory activity in itself or is capable of functioning as a prodrug of a compound having excellent CDK7 inhibitory activity, and is useful as a drug (e.g., a therapeutic drug and/or a prophylactic drug for cancers or inflammatory diseases). 

The invention claimed is:
 1. A compound represented by the formula (A1) or (A1′):

wherein P¹ and P² are each a benzyloxycarbonyl group. 